Home Other Building Blocks 2,2-Diphenylethylamine

2,2-Diphenylethylamine

CAS No.:
3963-62-0
Catalog Number:
AG0032X2
Molecular Formula:
C14H15N
Molecular Weight:
197.2756
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
96%
In Stock USA
United States
$13
- +
5g
96%
In Stock USA
United States
$32
- +
25g
96%
In Stock USA
United States
$119
- +
100g
96%
In Stock USA
United States
$344
- +
Product Description
Catalog Number:
AG0032X2
Chemical Name:
2,2-Diphenylethylamine
CAS Number:
3963-62-0
Molecular Formula:
C14H15N
Molecular Weight:
197.2756
MDL Number:
MFCD00008143
IUPAC Name:
2,2-diphenylethanamine
InChI:
InChI=1S/C14H15N/c15-11-14(12-7-3-1-4-8-12)13-9-5-2-6-10-13/h1-10,14H,11,15H2
InChI Key:
RXMTUVIKZRXSSM-UHFFFAOYSA-N
SMILES:
NCC(c1ccccc1)c1ccccc1
EC Number:
223-565-7
NSC Number:
27209
Properties
Complexity:
148  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
197.12g/mol
Formal Charge:
0
Heavy Atom Count:
15  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
197.281g/mol
Monoisotopic Mass:
197.12g/mol
Rotatable Bond Count:
3  
Topological Polar Surface Area:
26A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.1  
Literature
Title Journal
Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis. Bioorganic & medicinal chemistry letters 20101101
Synthesis, structure-affinity relationships, and modeling of AMDA analogs at 5-HT2A and H1 receptors: structural factors contributing to selectivity. Bioorganic & medicinal chemistry 20090915
NMDA receptor affinities of 1,2-diphenylethylamine and 1-(1,2-diphenylethyl)piperidine enantiomers and of related compounds. Bioorganic & medicinal chemistry 20090501
Potential modes of interaction of 9-aminomethyl-9,10-dihydroanthracene (AMDA) derivatives with the 5-HT2A receptor: a ligand structure-affinity relationship, receptor mutagenesis and receptor modeling investigation. Journal of medicinal chemistry 20081113
Structure-activity correlations for beta-phenethylamines at human trace amine receptor 1. Bioorganic & medicinal chemistry 20080801
Two- and three-dimensional quantitative structure-activity relationships studies on a series of liver x receptor ligands. The open medicinal chemistry journal 20080101
Quantification of cibenzoline by enzyme-linked immunosorbent assay. Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan 20070601
Geometry-affinity relationships of the selective serotonin receptor ligand 9-(aminomethyl)-9,10-dihydroanthracene. Journal of medicinal chemistry 20020411
Exploring the relationship between binding modes of 9-(aminomethyl)-9,10-dihydroanthracene and cyproheptadine analogues at the 5-HT2A serotonin receptor. Bioorganic & medicinal chemistry letters 20010226
Properties