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Details

Stereochemistry ACHIRAL
Molecular Formula C8H7ClO2
Molecular Weight 170.593
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Carbobenzoxy chloride

SMILES

ClC(=O)OCC1=CC=CC=C1

InChI

InChIKey=HSDAJNMJOMSNEV-UHFFFAOYSA-N
InChI=1S/C8H7ClO2/c9-8(10)11-6-7-4-2-1-3-5-7/h1-5H,6H2

HIDE SMILES / InChI
Molecular Formula C8H7ClO2
Molecular Weight 170.593
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
Chemoselective synthesis of sialic acid 1,7-lactones.
2010-08-20
Benzyl N-(4-pyrid-yl)carbamate.
2010-01-20
(3aS,7aS)-5-[(S)-3,3,3-Trifluoro-2-meth-oxy-2-phenyl-propano-yl]-2,3,4,5,6,7-hexa-hydro-1H-pyrrolo[3,4-c]pyridin-3(2H)-one monohydrate.
2009-12-16
Extended Grunwald-Winstein analysis - LFER used to gauge solvent effects in p-nitrophenyl chloroformate solvolysis.
2008-11
Benzyl 2,5-dioxopyrrolidin-1-yl carbonate.
2008-06-21
Preparation and addition--elimination reactions of benzyl alpha,beta,beta-trifluoroacrylate. A new stereoselective approach to (Z)-beta-substituted alpha,beta-difluoroacrylates.
2008-01-18
Zinc complexes of the biomimetic N,N,O ligand family of substituted 3,3-bis(1-alkylimidazol-2-yl)propionates: the formation of oxalate from pyruvate.
2007-11
A convenient allylsilane-N-acyliminium route toward indolizidine and quinolizidine alkaloids.
2007-10-02
FeSO4 x 7H2O-catalyzed four-component synthesis of protected homoallylic amines.
2007-07-06
Functionalization of N-[(silyl)methyl]-beta-lactam carbanions with carbon electrophiles.
2006-08-18
[Synthesis and antibacterial activity of (S) -5-acetylaminomethyl-3-[(4-substituted-aminomethyl) phenyl] -2-oxazolindinone derivatives].
2006-05
High yield regioselective monobenzyloxycarbonylation of secondary alcohols in glycopyranoside series.
2003-10-31
An improved synthesis of a trifurcated newkome-type monomer and orthogonally protected two-generation dendrons.
2002-02-22
Patents

Patents

04031071
3
04094863
2
04096263
8
04147780
7
04179569
6
04182769
5
04197240
11
04205085
7
04219559
28
04250085
3
04252803
2
04266025
2
04309442
6
04311705
1
04355037
9
04382143
3
04447436
4
04515717
14
04518532
6
04521514
1
04594196
1
04666906
2
04695575
5
04839374
5
04886894
3
04958036
1
04977159
4
04990504
7
05051420
1
05064861
7
05081130
1
05089518
4
05112966
2
JP2000086604A
2
JP2000302708A
1
JP2001233753A
4
JP2004203839A
3
JP2011001351A
4
JP2011177401A
2
JPH03218389A
1
JPH06234603A
3
JPH07173101A
1
JPH0717822A
1
JPH09169678A
1
JPH10130104A
2
JPH101453A
1
JPH10265437A
1
JPH11100351A
2
JPS5549361A
1
JPS5917997A
1
JPS6463565A
1
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:59:05 GMT 2025
Edited
by admin
on Mon Mar 31 19:59:05 GMT 2025
Record UNII
170BP0DD31
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BENZYL CHLOROFORMATE
HSDB  
Preferred Name English
Carbobenzoxy chloride
MI  
Common Name English
CARBONOCHLORIDIC ACID PHENYLMETHYL ESTER
Systematic Name English
NSC-83466
Code English
CARBOBENZOXY CHLORIDE [MI]
Common Name English
FORMIC ACID, CHLORO-, BENZYL ESTER
Common Name English
BENZYLCARBONYL CHLORIDE
Systematic Name English
BENZYL CHLOROFORMATE [HSDB]
Common Name English
CHLOROFORMIC ACID BENZYL ESTER
Systematic Name English
BENZYL CHLOROCARBONATE
Systematic Name English
Code System Code Type Description
MERCK INDEX
m3071
Created by admin on Mon Mar 31 19:59:05 GMT 2025 , Edited by admin on Mon Mar 31 19:59:05 GMT 2025
PRIMARY Merck Index
EPA CompTox
DTXSID9027158
Created by admin on Mon Mar 31 19:59:05 GMT 2025 , Edited by admin on Mon Mar 31 19:59:05 GMT 2025
PRIMARY
WIKIPEDIA
BENZYL CHLOROFORMATE
Created by admin on Mon Mar 31 19:59:05 GMT 2025 , Edited by admin on Mon Mar 31 19:59:05 GMT 2025
PRIMARY
ECHA (EC/EINECS)
207-925-0
Created by admin on Mon Mar 31 19:59:05 GMT 2025 , Edited by admin on Mon Mar 31 19:59:05 GMT 2025
PRIMARY
NSC
83466
Created by admin on Mon Mar 31 19:59:05 GMT 2025 , Edited by admin on Mon Mar 31 19:59:05 GMT 2025
PRIMARY
FDA UNII
170BP0DD31
Created by admin on Mon Mar 31 19:59:05 GMT 2025 , Edited by admin on Mon Mar 31 19:59:05 GMT 2025
PRIMARY
HSDB
364
Created by admin on Mon Mar 31 19:59:05 GMT 2025 , Edited by admin on Mon Mar 31 19:59:05 GMT 2025
PRIMARY
PUBCHEM
10387
Created by admin on Mon Mar 31 19:59:05 GMT 2025 , Edited by admin on Mon Mar 31 19:59:05 GMT 2025
PRIMARY
MESH
C018241
Created by admin on Mon Mar 31 19:59:05 GMT 2025 , Edited by admin on Mon Mar 31 19:59:05 GMT 2025
PRIMARY
CAS
501-53-1
Created by admin on Mon Mar 31 19:59:05 GMT 2025 , Edited by admin on Mon Mar 31 19:59:05 GMT 2025
PRIMARY
SMS_ID
300000053153
Created by admin on Mon Mar 31 19:59:05 GMT 2025 , Edited by admin on Mon Mar 31 19:59:05 GMT 2025
PRIMARY
NIH
NCATS
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