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107095-00-1

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107095-00-1 Usage

Description

N,2,3-Trimethyl-5-nitro-6-quinoxalinamine is a brown solid that is a mutagen itself and is used as a reagent to prepare other mutagens commonly found in food.

Uses

Used in Food Industry:
N,2,3-Trimethyl-5-nitro-6-quinoxalinamine is used as a reagent for preparing other mutagens commonly found in food, which can be used to study the effects of these mutagens on food safety and quality.
Used in Research and Development:
N,2,3-Trimethyl-5-nitro-6-quinoxalinamine is used as a mutagen itself in research and development, particularly in the field of genetics and molecular biology, to study the effects of mutagens on DNA and their potential applications in genetic engineering and gene therapy.

Check Digit Verification of cas no

The CAS Registry Mumber 107095-00-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,0,9 and 5 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 107095-00:
(8*1)+(7*0)+(6*7)+(5*0)+(4*9)+(3*5)+(2*0)+(1*0)=101
101 % 10 = 1
So 107095-00-1 is a valid CAS Registry Number.

107095-00-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N,2,3-trimethyl-5-nitroquinoxalin-6-amine

1.2 Other means of identification

Product number -
Other names 2,3-dimethyl-6-methylamino-5-nitroquinoxaline

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:107095-00-1 SDS

107095-00-1Relevant articles and documents

Synthesis of Mutagenic Methyl- and Phenyl-substituted 2-Amino-3H-imidazoquinoxalines via 2,1,3-Benzoselenadiazoles

Grivas, Spiros,Tian, Wei,Ronne, Erik,Lindstroem, Stefan,Olsson, Kjell

, p. 521 - 528 (2007/10/02)

2-Amino-3-methyl-3H-imidazoquinoxaline, all its derivatives with 1-4 methyl groups in positions 4, 5, 7 and 8, and 2-amino-3,5-dimethyl-7,8-diphenyl-3H-imidazoquinoxaline have been synthesized from the corresponding 6-methylamino-5-nitroquinoxalines through reduction and cyclization with cyanogen bromide.The quinoxalines were obtained from the appropriate α-dicarbonyl compounds and 4-methylamino-3-nitro-1,2-benzenediamines.The latter were prepared from 4-halo-1,2-benzenediamines via 2,1,3-benzoselenadiazoles.The 7- and 8-phenyl derivatives of 2-amino-3,5-dimethyl-3H-imidazoquinoxaline have been synthesized in a slightly different way.

Efficient synthesis of mutagenic imidazo[4,5-f] quinoxalin-2-amines via readily accessible 2,1,3-benzoselenadiazoles.

Grivas

, p. 404 - 406 (2007/10/02)

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