3,3-Diphenylpropylamine

3,3-Diphenylpropylamine

Names
Preferred IUPAC name 3,3-Diphenylpropan-1-amine
Identifiers
CAS Number	5586-73-2  Y
3D model (JSmol)	Interactive image
ChEMBL	ChEMBL609579  Y
ChemSpider	71998  Y
ECHA InfoCard	100.024.532
PubChem CID	79698
UNII	C31E561S64  Y
CompTox Dashboard (EPA)	DTXSID30204458
InChI InChI=1S/C15H17N/c16-12-11-15(13-7-3-1-4-8-13)14-9-5-2-6-10-14/h1-10,15H,11-12,16H2 Y Key: KISZTEOELCMZPY-UHFFFAOYSA-N Y
SMILES C1=CC=C(C=C1)C(CCN)C2=CC=CC=C2
Properties
Chemical formula	C15H17N
Molar mass	211.308 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N  verify  (what is  YN ?) Infobox references

3,3-Diphenylpropylamine is a form of diphenylpropylamine.

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

3,3-Diphenylpropylamine derivatives

Name	Identifier	Chemical structure
BIIA 0388	CID:9958467 [337359-07-6]
BZP derivative	[1]
Droprenilamine	[57653-27-7]
Delucemine	[186495-49-8 ]
Fendiline	[13042-18-7]
Lercanidipine	[100427-26-7]
KD-983	[50597-65-4]
Mepramidil	[23891-60-3]
Milverine	[75437-14-8]
PF 244	Fb: [52017-07-9]
Prenylamine	[390-64-7]
SoRI-20041	now SRI-20041
Tiopropamine	[39516-21-7]
CB1 receptor ligand	[117-34-0] [5586-73-2] [2]
5-APDI	[3]

References

1. Tadayuki Suzuki & Toshiharu Megumi, U.S. patent 3,957,790 (1976 to Tokyo Tanabe Co Ltd).
2. Urbani, P., Cascio, M. G., Ramunno, A., Bisogno, T., Saturnino, C., Marzo, V. D. (August 2008). "Novel sterically hindered cannabinoid CB1 receptor ligands". Bioorganic & Medicinal Chemistry. 16 (15): 7510–7515. doi:10.1016/j.bmc.2008.06.001. hdl: 11563/122572 . PMID   18579386.
3. Frank Troxler & Albert Hofman, OA01894 (1970 to Sandoz KK).