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Revision as of 17:42, 16 February 2012 editBeetstra (talk | contribs)Edit filter managers, Administrators172,031 edits Saving copy of the {{chembox}} taken from revid 456501646 of page 3,3-Diphenylpropylamine for the Chem/Drugbox validation project (updated: 'CASNo').  Latest revision as of 21:57, 16 October 2024 edit Innerstream (talk | contribs)Autopatrolled, Extended confirmed users4,049 editsmNo edit summary 
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{{cs1 config|name-list-style=vanc}}
{{ambox | text = This page contains a copy of the infobox ({{tl|chembox}}) taken from revid of page ] with values updated to verified values.}}
{{chembox {{chembox
| Verifiedfields = changed | Verifiedfields = changed
| Watchedfields = changed
| verifiedrevid = 456500605 | verifiedrevid = 477217252
|ImageFile=3,3-diphenylpropylamine.svg | ImageFile=3,3-diphenylpropylamine.svg
|ImageSize=200px | ImageSize=200px
|IUPACName=
| PIN=3,3-Diphenylpropan-1-amine
|OtherNames= | OtherNames=
|Section1={{Chembox Identifiers |Section1={{Chembox Identifiers
| CASNo_Ref = {{cascite|changed|??}} | CASNo_Ref = {{cascite|correct|CAS}}
| CASNo = <!-- blanked - oldvalue: 5586-73-2 --> | CASNo=5586-73-2
| ChEMBL_Ref = {{ebicite|correct|EBI}} | UNII_Ref = {{fdacite|correct|FDA}}
| UNII = C31E561S64
| ChEMBL_Ref = {{ebicite|correct|EBI}}
| ChEMBL = 609579 | ChEMBL = 609579
| PubChem=79698 | PubChem=79698
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 71998 | ChemSpiderID = 71998
| StdInChI_Ref = {{stdinchicite|correct|chemspider}} | StdInChI_Ref = {{stdinchicite|correct|chemspider}}
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}} }}
|Section2={{Chembox Properties |Section2={{Chembox Properties
| C=15|H=17|N=1 | C=15 | H=17 | N=1
| Appearance= | Appearance=
| Density= | Density=
| MeltingPt= | MeltingPt=
| BoilingPt= | BoilingPt=
| Solubility= | Solubility=
}} }}
|Section3={{Chembox Hazards |Section3={{Chembox Hazards
| MainHazards= | MainHazards=
| FlashPt= | FlashPt=
| AutoignitionPt =
| Autoignition=
}} }}
}} }}

'''3,3-Diphenylpropylamine''' is a form of ].

It is commonly conjugated to another agent giving a "bifunctional" molecule. Some such agents are used to treat ]s.

{| class="wikitable"
|+ 3,3-Diphenylpropylamine derivatives
|-
! Name !! Identifier!!Chemical structure
|-
| ] || || ]
|-
| ] derivative || <ref>Tadayuki Suzuki & Toshiharu Megumi, {{US patent|3957790}} (1976 to Tokyo Tanabe Co Ltd).</ref> || ]
|-
| ] || || ]
|-
| ] || || ]
|-
| ]|| || ]
|-
| ] || || ]
|-
| ] || || ]
|-
| ] || || ]
|-
| ] || || ]
|-
| ] || Fb: || ]
|-
| ] || || ]
|-
| ] || now SRI-20041 || ]
|-
| ] || || ]
|-
| CB1 receptor ligand || <ref>{{cite journal | vauthors=((Urbani, P.)), ((Cascio, M. G.)), ((Ramunno, A.)), ((Bisogno, T.)), ((Saturnino, C.)), ((Marzo, V. D.)) | journal=Bioorganic & Medicinal Chemistry | title=Novel sterically hindered cannabinoid CB1 receptor ligands | volume=16 | issue=15 | pages=7510–7515 | date= August 2008 | doi=10.1016/j.bmc.2008.06.001| pmid=18579386 | hdl=11563/122572 | hdl-access=free }}</ref> || ]
|}
{{clear}}


==References==
{{reflist}}

{{DEFAULTSORT:Diphenylpropylamine, 3,3-}}
]


{{amine-stub}}