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Details

Stereochemistry ACHIRAL
Molecular Formula C7H5ClO2
Molecular Weight 156.566
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Phenyl chloroformate

SMILES

ClC(=O)OC1=CC=CC=C1

InChI

InChIKey=AHWALFGBDFAJAI-UHFFFAOYSA-N
InChI=1S/C7H5ClO2/c8-7(9)10-6-4-2-1-3-5-6/h1-5H

HIDE SMILES / InChI
Molecular Formula C7H5ClO2
Molecular Weight 156.566
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Unknown
149124
PubMed

PubMed

TitleDatePubMed
Dendritic polyglycerols with oligoamine shells show low toxicity and high siRNA transfection efficiency in vitro.
2010-10-20
Analysis of the nucleophilic solvation effects in isopropyl chlorothioformate solvolysis.
2010-06-29
Design of group IIA secreted/synovial phospholipase A(2) inhibitors: an oxadiazolone derivative suppresses chondrocyte prostaglandin E(2) secretion.
2010-06-01
Use of empirical correlations to determine solvent effects in the solvolysis of S-methyl chlorothioformate.
2010-05-25
Synthesis and characterization of polycarbonates by melt phase interchange reactions of alkylene and arylene diacetates with alkylene and arylene diphenyl dicarbonates.
2010-05-18
Development of chiral thiourea catalysts and its application to asymmetric catalytic reactions.
2010-05
Phenyl N-cyclo-hexyl-carbamate.
2009-12-04
Phenyl piperidine-1-carboxyl-ate.
2009-12-04
Phenyl N-(4-methoxy-phen-yl)carbamate.
2009-07-25
Phenyl N-(2-methyl-phen-yl)carbamate.
2009-06-20
Phenyl N-(p-tol-yl)carbamate.
2009-06-17
Phenyl N-(1,3-thia-zol-2-yl)carbamate.
2009-06-06
Phenyl N-phenyl-carbamate.
2009-05-23
Phenyl N-(4-fluorophen-yl)carbamate.
2009-04-18
Corrrelation of the specific rates of solvolysis of ethyl fluoroformate using the extended Grunwald-Winstein equation.
2009-03
Grunwald-Winstein analysis: isopropyl chloroformate solvolysis revisited.
2009-03
Phenyl N-[4-chloro-3-(trifluoro-meth-yl)phen-yl]carbamate.
2009-02-18
Extended Grunwald-Winstein analysis - LFER used to gauge solvent effects in p-nitrophenyl chloroformate solvolysis.
2008-11
1-Benzyl-3-(2-furylmeth-yl)-1,2,3,4,5,6-hexa-hydro-spiro-[benzo[h]quinazoline-5,1'-cyclo-hexa-ne]-2,4-dione.
2008-03-29
The first solid enols of anhydrides. Structure, properties, and enol/anhydride equilibria(1).
2007-11-23
Role of the counterion in the effects of added ethylene glycol to aqueous alkyltrimethylammonium micellar solutions.
2006-06-15
Ionizing power and nucleophilicity in water in oil AOT-based microemulsions.
2005-08-16
Synthesis of a biotin-conjugate of phosmidosine O-ethyl ester as a G1 arrest antitumor drug.
2004-12-15
Conductometric, surface tension, and kinetic studies in mixed SDS-Tween 20 and SDS-SB3-12 micellar solutions.
2004-12-07
Kinetic study in water-ethylene glycol cationic, zwitterionic, nonionic, and anionic micellar solutions.
2004-11-09
Indium mediated allylation of quinoline and isoquinoline activated by phenyl chloroformate.
2004-08-07
A practical synthesis of cabergoline.
2002-10-04
Patents

Patents

04101663
6
04107435
2
04119717
1
04123450
1
04131674
4
04154840
20
04166120
1
04187100
1
04198417
1
04220646
17
04268514
7
04345081
2
04345934
2
04355037
9
04374137
2
04375471
1
04408053
9
04409229
1
04451467
1
04454340
1
04456605
1
04459150
1
04460584
3
04466964
1
04480101
2
04501860
1
04507311
1
04510156
1
04542142
8
04542213
1
04551474
1
04604397
4
04670447
4
04694004
2
04728355
1
04764616
6
04775761
8
04788201
1
04806649
8
JP2000143755A
1
JP2000143756A
1
JP2000327936A
1
JP2000344780A
1
JP2002539206A
3
JP2006518367A
3
JP4771442B2
1
JPH03264569A
1
JPH0761956A
1
JPH09221464A
1
JPH10245366A
1
JPS06147480A
1
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:36:48 GMT 2025
Edited
by admin
on Mon Mar 31 19:36:48 GMT 2025
Record UNII
6TND0D6D3Y
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-210946
Preferred Name English
Phenyl chloroformate
Systematic Name English
PHENYLCHLOROFORMIC ACID
Systematic Name English
PHENYL CHLOROCARBONATE
Systematic Name English
PHENYLOXYCARBONYL CHLORIDE
Systematic Name English
FORMIC ACID, CHLORO-, PHENYL ESTER
Systematic Name English
CHLOROFORMIC ACID PHENYL ESTER
Systematic Name English
PHENYL CARBONOCHLORIDATE
Systematic Name English
CARBONOCHLORIDIC ACID, PHENYL ESTER
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID9044403
Created by admin on Mon Mar 31 19:36:48 GMT 2025 , Edited by admin on Mon Mar 31 19:36:48 GMT 2025
PRIMARY
ECHA (EC/EINECS)
217-547-8
Created by admin on Mon Mar 31 19:36:48 GMT 2025 , Edited by admin on Mon Mar 31 19:36:48 GMT 2025
PRIMARY
CAS
1885-14-9
Created by admin on Mon Mar 31 19:36:48 GMT 2025 , Edited by admin on Mon Mar 31 19:36:48 GMT 2025
PRIMARY
PUBCHEM
15891
Created by admin on Mon Mar 31 19:36:48 GMT 2025 , Edited by admin on Mon Mar 31 19:36:48 GMT 2025
PRIMARY
FDA UNII
6TND0D6D3Y
Created by admin on Mon Mar 31 19:36:48 GMT 2025 , Edited by admin on Mon Mar 31 19:36:48 GMT 2025
PRIMARY
NSC
210946
Created by admin on Mon Mar 31 19:36:48 GMT 2025 , Edited by admin on Mon Mar 31 19:36:48 GMT 2025
PRIMARY
NIH
NCATS
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