2-METHYL-2-NITROSOPROPANE

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NCATS

Details

Stereochemistry	ACHIRAL
Molecular Formula	C4H9NO
Molecular Weight	87.1204
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of 2-METHYL-2-NITROSOPROPANE

SMILES

CC(C)(C)N=O

InChI

InChIKey=LUQZKEZPFQRRRK-UHFFFAOYSA-N

InChI=1S/C4H9NO/c1-4(2,3)5-6/h1-3H3

HIDE SMILES / InChI

Molecular Formula	C4H9NO
Molecular Weight	87.1204
Charge	0
Count	MOL RATIO 1 MOL RATIO (average)

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

Approval Year

PubMed

Show entries

Title	Date	PubMed
Phenylbutazone radicals inactivate creatine kinase.	2001 Feb	11264893
ESR-spin trapping study on the sonochemistry of liquids in the presence of oxygen. Evidence for the superoxide radical anion formation.	2001 Jan	11105318
Inactivation of creatine kinase during the interaction of indomethacin with horseradish peroxidase and hydrogen peroxide: involvement of indomethacin radicals.	2001 Mar 14	11248219
Identification of protein-derived tyrosyl radical in the reaction of cytochrome c and hydrogen peroxide: characterization by ESR spin-trapping, HPLC and MS.	2002 Apr 15	11931655
Protein oxidation of cytochrome C by reactive halogen species enhances its peroxidase activity.	2002 Aug 16	12050149

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Patents

Substance Class	Chemical
Record UNII	JGX6N17V2U
Record Status	`Validated (UNII)`
Record Version

Show entries

Name

Type

Language

2-METHYL-2-NITROSOPROPANE

Systematic Name

English

2-NITROSO-2-METHYLPROPANE

Systematic Name

English

NITROSO-TERT-BUTANE

Systematic Name

English

TRIMETHYLNITROSOMETHANE

Systematic Name

English

NSC-150348

Code

English

Showing 1 to 5 of 7 entries

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Code System

Code

Type

Description

WIKIPEDIA

2-METHYL-2-NITROSOPROPANE

PRIMARY

CAS

917-95-3

PRIMARY

FDA UNII

JGX6N17V2U

PRIMARY

NSC

150348

PRIMARY

PUBCHEM

23272

PRIMARY

Showing 1 to 5 of 5 entries