Revision as of 13:35, 15 February 2012 editBeetstra (talk | contribs)Edit filter managers, Administrators172,031 edits Saving copy of the {{chembox}} taken from revid 474663576 of page Acridine_orange for the Chem/Drugbox validation project (updated: 'ChEBI', 'KEGG', 'CASNo').← Previous edit |
Revision as of 13:35, 15 February 2012 edit undoBeetstra (talk | contribs)Edit filter managers, Administrators172,031 edits Saving copy of the {{chembox}} taken from revid 472296269 of page Aluminium_borohydride for the Chem/Drugbox validation project (updated: 'CASNo').Next edit → |
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{{ambox | text = This page contains a copy of the infobox ({{tl|chembox}}) taken from revid of page ] with values updated to verified values.}} |
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{{ambox | text = This page contains a copy of the infobox ({{tl|chembox}}) taken from revid of page ] with values updated to verified values.}} |
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{{Chembox |
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{{chembox |
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| verifiedrevid = 427611348 |
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| Verifiedfields = changed |
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| ImageFile = Aluminium-borohydride-2D-from-xtal.png |
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| verifiedrevid = 457803101 |
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| ImageSize = |
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| ImageFile = Acridine Orange.png |
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| ImageName = Acridine orange |
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| ImageName = Structural formula of the aluminium borohydride molecule |
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| IUPACName = Aluminium borohydride |
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| PIN = ''N'',''N'',''N<nowiki>'</nowiki>'',''N<nowiki>'</nowiki>''-Tetramethylacridine-3,6-diamine |
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| OtherNames = Aluminum borohydride, aluminium tetrahydroborate, aluminum tetrahydroborate |
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| SystematicName = 3-''N'',3-''N'',6-''N'',6-''N''-Tetramethylacridine-3,6-diamine |
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| Reference = <ref name="hand"> |
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| OtherNames = 3,6-Acridinediamine<br /> |
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{{Cite book |
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Acridine Orange Base<br /> |
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| last = Lide |
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Acridine Orange NO<br /> |
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| first = David R. |
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Basic Orange 14<br /> |
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| author-link = |
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Euchrysine<br /> |
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| last2 = |
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Rhoduline Orange<br /> |
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| first2 = |
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Rhoduline Orange N<br /> |
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| author2-link = |
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Rhoduline Orange NO<br /> |
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| publication-date = |
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Solvent Orange 15<br /> |
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| date = |
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Waxoline Orange A |
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| year = 1998 |
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| title = Handbook of Chemistry and Physics |
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| edition = 87 |
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| volume = |
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| series = |
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| publication-place = Boca Raton, FL |
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| place = |
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| publisher = CRC Press |
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| id = |
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| isbn = 0-8493-0594-2 |
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| doi = |
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| oclc = |
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| pages = 4–39 |
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| url = |
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| accessdate = |
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}}</ref> |
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| Section1 = {{Chembox Identifiers |
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| Section1 = {{Chembox Identifiers |
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| ChEMBL_Ref = {{ebicite|correct|EBI}} |
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| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
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| ChEMBL = 81880 |
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| ChemSpiderID = 55734 |
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| InChI = 1/Al.3BH4/h;3*1H4/q+3;3*-1 |
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| InChIKey = LNJYEMMRSAGORU-UHFFFAOYAC |
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| SMILES = ... |
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| StdInChI_Ref = {{stdinchicite|correct|chemspider}} |
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| StdInChI_Ref = {{stdinchicite|correct|chemspider}} |
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| StdInChI = 1S/C17H19N3/c1-19(2)14-7-5-12-9-13-6-8-15(20(3)4)11-17(13)18-16(12)10-14/h5-11H,1-4H3 |
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| StdInChI = 1S/Al.3BH4/h;3*1H4/q+3;3*-1 |
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| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} |
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| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} |
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| StdInChIKey = DPKHZNPWBDQZCN-UHFFFAOYSA-N |
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| StdInChIKey = LNJYEMMRSAGORU-UHFFFAOYSA-N |
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| CASNo = <!-- blanked - oldvalue: 16962-07-5 --> |
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| CASNo_Ref = {{cascite|changed|??}} |
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| CASNo_Ref = {{cascite|correct|??}}= |
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| CASNo = <!-- blanked - oldvalue: 494-38-2 --> |
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| PubChem = 62344 |
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| RTECS = |
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| EINECS = |
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| PubChem_Ref = {{Pubchemcite}} |
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| ChemSpiderID = 56136 |
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| PubChem = |
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}} |
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| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
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| EINECS = 200-614-0 |
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| MeSHName = Acridine+orange |
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| ChEBI_Ref = {{ebicite|changed|EBI}} |
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| ChEBI = <!-- blanked - oldvalue: 234241 --> |
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| RTECS = AR7601000 |
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| SMILES = n1c3c(cc2c1cc(N(C)C)cc2)ccc(c3)N(C)C |
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| InChI = 1/C17H19N3/c1-19(2)14-7-5-12-9-13-6-8-15(20(3)4)11-17(13)18-16(12)10-14/h5-11H,1-4H3 |
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| InChIKey = DPKHZNPWBDQZCN-UHFFFAOYAJ |
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| KEGG_Ref = {{keggcite|changed|kegg}} |
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| KEGG = <!-- blanked - oldvalue: C19315 --> |
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}} |
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| Section2 = {{Chembox Properties |
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| Section2 = {{Chembox Properties |
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|C=17|H=19|N=3| |
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| Al = 1 | B = 3 | H = 12 |
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| Appearance = Orange powder |
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| Appearance = colorless liquid |
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| Density = |
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}} |
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| MeltingPtC = -64.5 |
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| Section7 = {{Chembox Hazards |
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| BoilingPtC = 44.5 |
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| EUClass = {{Hazchem_Xi}} {{Hazchem_N}} |
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| NFPA-H = 2 |
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| Solubility = reacts |
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}} |
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| NFPA-F = 0 |
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| Section3 = {{Chembox Structure |
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| NFPA-R = 0 |
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| CrystalStruct = |
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| SPhrases = {{S26}} {{S28}} {{S37}} {{S45}} |
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| Coordination = |
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| MolShape = |
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| Section4 = {{Chembox Hazards |
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| EUClass = |
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| FlashPt = Spontaneously ignites |
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| NFPA-H = |NFPA-F = |NFPA-R = |
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}} |
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}} |
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}} |