P-ACETOXYNITROBENZENE

Details

Stereochemistry	ACHIRAL
Molecular Formula	C8H7NO4
Molecular Weight	181.1455
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

SMILES

CC(=O)OC1=CC=C(C=C1)[N+]([O-])=O

InChI

InChIKey=QAUUDNIGJSLPSX-UHFFFAOYSA-N

InChI=1S/C8H7NO4/c1-6(10)13-8-4-2-7(3-5-8)9(11)12/h2-5H,1H3

HIDE SMILES / InChI

Approval Year

Targets

Targets

Primary Target	Pharmacology	Condition	Potency
Carbonic anhydrase I 62	Substrate 661
Carbonic anhydrase XIII 10	Substrate 661
Acyl coenzyme A:cholesterol acyltransferase 15	Substrate 661
Carbonic anhydrase III 2	Substrate 661

PubMed

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Title	Date	PubMed
cDNA cloning, characterization and stable expression of novel human brain carboxylesterase.	1999 Sep 10	10518925
Multiple isotope effects on the acyl group transfer reactions of amides and esters.	2001 Apr	11308302
The oxidative mechanism of heparin interferes with radical production by glucose and reduces the degree of glycooxidative modifications on human serum albumin.	2001 Apr	11298735
Assay of serum arylesterase activity by fitting to the reaction curve with an integrated rate equation.	2001 Dec	11718680
Purification and characterisation of an ester hydrolase from a strain of Arthrobacter species: its application in asymmetrisation of 2-benzyl-1,3-propanediol acylates.	2001 Feb	11249119

Showing 1 to 5 of 38 entries

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Patents

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Name

Type

Language

NSC-2633

Preferred Name

English

P-ACETOXYNITROBENZENE

Common Name

English

ACETIC ACID, P-NITROPHENYL ESTER

Systematic Name

English

PHENOL, P-NITRO-, ACETATE

Systematic Name

English

P-NITROPHENOL ACETATE

Common Name

English

Showing 1 to 5 of 8 entries

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Code System

Code

Type

Description

ECHA (EC/EINECS)

212-593-5

PRIMARY

NSC

2633

PRIMARY

PUBCHEM

13243

PRIMARY

FDA UNII

I902J0QH9S

PRIMARY

EPA CompTox

DTXSID2061191

PRIMARY

Showing 1 to 5 of 7 entries

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SUBSTANCE RECORD


					I902J0QH9S

P-ACETOXYNITROBENZENE