Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C13H13N.ClH |
| Molecular Weight | 219.71 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.NC(C1=CC=CC=C1)C2=CC=CC=C2
InChI
InChIKey=CIHWJRSPVJBHGT-UHFFFAOYSA-N
InChI=1S/C13H13N.ClH/c14-13(11-7-3-1-4-8-11)12-9-5-2-6-10-12;/h1-10,13H,14H2;1H
| Molecular Formula | ClH |
| Molecular Weight | 36.461 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | C13H13N |
| Molecular Weight | 183.249 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Physicochemical and chromatographic evaluation of benzhydrylamine-resin as an anion exchanger solid support. | 2003 Jul 31 |
|
| Novel 4-alkyl-1-arylpiperazines and 1,2,3,4-tetrahydroisoquinolines containing diphenylmethylamino or diphenylmethoxy fragment with differentiated 5-HT1A/5-HT2A/D2 receptor activity. | 2003 Jul-Aug |
|
| 4-(4-Bromo-benzyl-ideneamino)-1-(diphenyl-amino-meth-yl)-3-[1-(4-isobutyl-phen-yl)eth-yl]-1H-1,2,4-triazole-5(4H)-thione. | 2008 May 7 |
|
| Design and combinatorial synthesis of a library of methylenesulfonamides and related compounds as potential kinase inhibitors. | 2009 Mar |
|
| Benzhydrylamine linker grafting: a strategy for the improved synthesis of C-terminal peptide amides. | 2010 Oct |
|
| Synthesis and comparative properties of two amide-generating resin linkers for use in solid phase peptide synthesis. | 2010 Oct |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 11:52:38 GMT 2023
by
admin
on
Sat Dec 16 11:52:38 GMT 2023
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| Record UNII |
LZ568SDT78
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| Record Status |
Validated (UNII)
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| Record Version |
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