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4-Nitro-5-methylamino-6-methyl-2,1,3-benzoselenodiazole, with the CAS number 149703-56-0, is a chemical compound that is characterized as a brown solid. It is primarily utilized in the field of organic synthesis, where it serves as a valuable building block for the creation of more complex molecules and compounds.

149703-56-0

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149703-56-0 Usage

Uses

Used in Organic Synthesis:
4-Nitro-5-methylamino-6-methyl-2,1,3-benzoselenodiazole is used as a synthetic intermediate for the development of various organic compounds. Its unique structure and functional groups make it a versatile component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-nitro-5-methylamino-6-methyl-2,1,3-benzoselenodiazole is used as a key component in the synthesis of novel drug candidates. Its presence in the molecular structure can potentially influence the pharmacological properties, such as activity, selectivity, and bioavailability, of the final drug product.
Used in Agrochemical Industry:
4-Nitro-5-methylamino-6-methyl-2,1,3-benzoselenodiazole is also employed in the agrochemical industry as a starting material for the synthesis of new pesticides, herbicides, and other crop protection agents. Its incorporation into these molecules can lead to improved efficacy, selectivity, and environmental safety.
Used in Dye and Pigment Industry:
In the dye and pigment industry, 4-nitro-5-methylamino-6-methyl-2,1,3-benzoselenodiazole is used as a building block for the development of new colorants with enhanced properties, such as improved color strength, lightfastness, and stability.
Used in Material Science:
4-Nitro-5-methylamino-6-methyl-2,1,3-benzoselenodiazole can be utilized in the field of material science for the synthesis of advanced materials with specific properties, such as conductivity, magnetism, or optical activity. Its integration into these materials can lead to the development of innovative applications in electronics, sensors, and other high-tech industries.

Check Digit Verification of cas no

The CAS Registry Mumber 149703-56-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,7,0 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 149703-56:
(8*1)+(7*4)+(6*9)+(5*7)+(4*0)+(3*3)+(2*5)+(1*6)=150
150 % 10 = 0
So 149703-56-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H8N4O2Se/c1-4-3-5-7(11-15-10-5)8(12(13)14)6(4)9-2/h3,9H,1-2H3

149703-56-0SDS

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,6-dimethyl-4-nitro-2,1,3-benzoselenadiazol-5-amine

1.2 Other means of identification

Product number -
Other names 4-Nitro-5-methylamino-6-methyl-2,1,3-benzoselenodiazole

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:149703-56-0 SDS

149703-56-0Relevant academic research and scientific papers

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.

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