2-NITRO-P-CRESOL

CC1=CC=C(O)C(=C1)[N+]([O-])=O

InChIKey=SYDNSSSQVSOXTN-UHFFFAOYSA-N

InChI=1S/C7H7NO3/c1-5-2-3-7(9)6(4-5)8(10)11/h2-4,9H,1H3

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

PubMed

Title	Date	PubMed
Investigations on the gas-phase photolysis and OH radical kinetics of methyl-2-nitrophenols.	2007-11-14	17960257
Abatement and degradation pathways of toluene in indoor air by positive corona discharge.	2007-08	17490711
Solid-phase microextraction and gas chromatography-mass spectrometry for analysis of phenols and nitrophenols in rainwater, as their t-butyldimethylsilyl derivatives.	2007-04	17260132
Effect of natural phenol derivatives on skeletal type sarcoplasmic reticulum Ca2+ -ATPase and ryanodine receptor.	2007	17641978
Spatial and geographical variations of urban, suburban and rural atmospheric concentrations of phenols and nitrophenols.	2006-03	16612896
Metabolism and excretion of 2-nitro-p-cresol in rats.	2002-12	12451443

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 20:35:26 GMT 2025` Edited by `admin` on `Mon Mar 31 20:35:26 GMT 2025`
Record UNII	P92KPK2NL3
Record Status	`Validated (UNII)`
Record Version

Name

Type

Language

NSC-5387

Preferred Name

English

2-NITRO-P-CRESOL

Common Name

English

PHENOL, 4-METHYL-2-NITRO-

Systematic Name

English

P-CRESOL, 2-NITRO-

Common Name

English

2-NITRO-4-METHYLPHENOL

Systematic Name

English

4-HYDROXY-3-NITROTOLUENE

Systematic Name

English

O-NITRO-P-METHYLPHENOL

Common Name

English

Code System Code Type Description

CAS

119-33-5