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Details

Stereochemistry ACHIRAL
Molecular Formula C7H4ClNO3
Molecular Weight 185.565
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of P-NITROBENZOYL CHLORIDE

SMILES

[O-][N+](=O)C1=CC=C(C=C1)C(Cl)=O

InChI

InChIKey=SKDHHIUENRGTHK-UHFFFAOYSA-N
InChI=1S/C7H4ClNO3/c8-7(10)5-1-3-6(4-2-5)9(11)12/h1-4H

HIDE SMILES / InChI

Molecular Formula C7H4ClNO3
Molecular Weight 185.565
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Bis[3α,7α,12α-tris-(4-nitro-benzo-yloxy)-5β-cholan-24-yl] disulfide-ethyl acetate-n-hexane (4/4/1).
2010-12-11
1,8-Bis(4-amino-benzo-yl)-2,7-dimeth-oxy-naphthalene.
2010-10-23
N-(Diethyl-carbamothio-yl)-4-nitro-benzamide.
2010-09-18
N-[(Morpholin-4-yl)carbonothio-yl]-4-nitro-benzamide.
2010-05-22
N-Cyclo-hexyl-N'-(4-nitro-benzo-yl)thio-urea.
2010-04-10
Ethyl 2-[3-(4-nitro-benzo-yl)thio-ureido]benzoate.
2010-03-31
Novel amidino substituted 2-phenylbenzothiazoles: synthesis, antitumor evaluation in vitro and acute toxicity testing in vivo.
2010-02
1,2-Bis(4-nitro-benzo-yl)hydrazine.
2009-08-19
1-(Benzothia-zol-2-yl)-3-(4-nitro-benzo-yl)thio-urea.
2009-08-08
1-(4-Bromo-phen-yl)-1-(4-nitro-benzo-yl)thio-urea.
2009-07-15
Spectrophotometric Quantitation of Metformin in Bulk Drug and Pharmaceutical Formulations using Multivariate Technique.
2009-05
Spectrophotometric method for analysis of metformin hydrochloride.
2009-01
(±)-Cyclo-hexane-1,2-diyl bis-(4-nitro-benzoate).
2008-10-22
1-(4-Nitro-benzo-yl)-3-(4-nitro-phen-yl)-thio-urea acetone hemisolvate.
2008-10-18
Preparation, GIAO NMR calculations and acidic properties of some novel 4,5-dihydro-1H-1,2,4-triazol-5-one derivatives with their antioxidant activities.
2008-01
2-(Methoxy-meth-oxy)-1-(4-oxobicyclo-[3.1.0]hexan-1-yl)ethyl 4-nitro-benzoate.
2007-12-21
Liquid chromatography-mass spectrometric assay of androstenediol in prostatic tissue: influence of androgen deprivation therapy on its level.
2006-11
Procedure for increasing the detection responses of estrogens in LC-MS based on introduction of a nitrobenzene moiety followed by electron capture atmospheric pressure chemical ionization.
2006-10
Studies on neurosteroids XVIII LC-MS analysis of changes in rat brain and serum testosterone levels induced by immobilization stress and ethanol administration.
2006-07
Novel benzofuran derivatives for PET imaging of beta-amyloid plaques in Alzheimer's disease brains.
2006-05-04
Mechanisms of solvolyses of acid chlorides and chloroformates. Chloroacetyl and phenylacetyl chloride as similarity models.
2005-10-28
HPLC determination of salinomycin and related compounds in fermentation media of Streptomyces albus and premixes.
2005-09-15
Ultraviolet derivatization of steroidal saponin in garlic and commercial garlic products as p-nitrobenzoate for liquid chromatographic determination.
2004-10-21
[Determination of sucralose in foods by HPLC using pre-column derivatization].
2002-10
HPLC simultaneous determination of glycerol and mannitol in human tissues for forensic analysis.
2002-02-18
A new approach for dynamics of enzyme-catalyzed glutathione conjugation by electrospray quadrupole/time-of-flight mass spectrometry.
2001-11-01
Synthesis of 1,2,4-triazino[5,6-b] indoles bearing 1,2,4-triazine moiety.
2001-06-22
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:34:07 GMT 2025
Edited
by admin
on Mon Mar 31 19:34:07 GMT 2025
Record UNII
X3H8PW2GC4
Record Status Validated (UNII)
Record Version
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Name Type Language
P-NITROBENZOYL CHLORIDE
Common Name English
4-NITROBENZOYL CHLORIDE
MI  
Preferred Name English
NITROBENZOYL CHLORIDE, P-
Common Name English
4-NITROBENZOIC ACID CHLORIDE
Systematic Name English
NSC-5381
Code English
4-NITROBENZOYL CHLORIDE [MI]
Common Name English
Code System Code Type Description
MERCK INDEX
m7947
Created by admin on Mon Mar 31 19:34:07 GMT 2025 , Edited by admin on Mon Mar 31 19:34:07 GMT 2025
PRIMARY Merck Index
NSC
5381
Created by admin on Mon Mar 31 19:34:07 GMT 2025 , Edited by admin on Mon Mar 31 19:34:07 GMT 2025
PRIMARY
PUBCHEM
8502
Created by admin on Mon Mar 31 19:34:07 GMT 2025 , Edited by admin on Mon Mar 31 19:34:07 GMT 2025
PRIMARY
FDA UNII
X3H8PW2GC4
Created by admin on Mon Mar 31 19:34:07 GMT 2025 , Edited by admin on Mon Mar 31 19:34:07 GMT 2025
PRIMARY
EPA CompTox
DTXSID9025742
Created by admin on Mon Mar 31 19:34:07 GMT 2025 , Edited by admin on Mon Mar 31 19:34:07 GMT 2025
PRIMARY
CAS
122-04-3
Created by admin on Mon Mar 31 19:34:07 GMT 2025 , Edited by admin on Mon Mar 31 19:34:07 GMT 2025
PRIMARY
ECHA (EC/EINECS)
204-517-4
Created by admin on Mon Mar 31 19:34:07 GMT 2025 , Edited by admin on Mon Mar 31 19:34:07 GMT 2025
PRIMARY