Details
Stereochemistry | ACHIRAL |
Molecular Formula | C8H7ClO |
Molecular Weight | 154.594 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
ClC(=O)CC1=CC=CC=C1
InChI
InChIKey=VMZCDNSFRSVYKQ-UHFFFAOYSA-N
InChI=1S/C8H7ClO/c9-8(10)6-7-4-2-1-3-5-7/h1-5H,6H2
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Synthesis and antimicrobial activity of some new sugar-based monocyclic beta-lactams. | 2004 Jan 31 |
|
Mechanisms of solvolyses of acid chlorides and chloroformates. Chloroacetyl and phenylacetyl chloride as similarity models. | 2005 Oct 28 |
|
A study on 4-acylamino-4,5-dihydro-1H-1,2,4-triazol-5-ones. | 2007 Aug 13 |
|
N,N-Diethyl-N'-phenyl-acetyl-thio-urea. | 2008 Nov 8 |
|
Synthesis and Pharmacological Evaluation of Azetidin-2-ones and Thiazolidin-4-ones Encompassing Benzothiazole. | 2008 Sep |
|
Synthesis and evaluation of 1-(1-(Benzo[b]thiophen-2-yl)cyclohexyl)piperidine (BTCP) analogues as inhibitors of trypanothione reductase. | 2009 Aug |
|
Penicillin Acylase-Catalyzed Effective and Stereoselective Acylation of 1-phenylethylamine in Aqueous Medium using Non-Activated Acyl Donor. | 2010 Apr |
|
Analysis of the nucleophilic solvation effects in isopropyl chlorothioformate solvolysis. | 2010 Jun 29 |
|
Use of empirical correlations to determine solvent effects in the solvolysis of S-methyl chlorothioformate. | 2010 May 25 |
Name | Type | Language | ||
---|---|---|---|---|
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Code | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Code | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
103-80-0
Created by
admin on Fri Dec 15 18:09:37 GMT 2023 , Edited by admin on Fri Dec 15 18:09:37 GMT 2023
|
PRIMARY | |||
|
7679
Created by
admin on Fri Dec 15 18:09:37 GMT 2023 , Edited by admin on Fri Dec 15 18:09:37 GMT 2023
|
PRIMARY | |||
|
DTXSID6059281
Created by
admin on Fri Dec 15 18:09:37 GMT 2023 , Edited by admin on Fri Dec 15 18:09:37 GMT 2023
|
PRIMARY | |||
|
T30899DRND
Created by
admin on Fri Dec 15 18:09:37 GMT 2023 , Edited by admin on Fri Dec 15 18:09:37 GMT 2023
|
PRIMARY | |||
|
203-146-5
Created by
admin on Fri Dec 15 18:09:37 GMT 2023 , Edited by admin on Fri Dec 15 18:09:37 GMT 2023
|
PRIMARY |
SUBSTANCE RECORD