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146177-58-4

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146177-58-4 Usage

Structure

Heterocyclic aromatic compound containing imidazole and quinoxaline rings

Pharmaceutical Relevance

Investigated for anticancer and antifungal properties

Enzyme Inhibition

Studied for inhibiting 3C protease, essential for certain virus replication

Fluorescent Probe

Potential for DNA and RNA detection

Applications

Biomedical and pharmaceutical potential

Check Digit Verification of cas no

The CAS Registry Mumber 146177-58-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,1,7 and 7 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 146177-58:
(8*1)+(7*4)+(6*6)+(5*1)+(4*7)+(3*7)+(2*5)+(1*8)=144
144 % 10 = 4
So 146177-58-4 is a valid CAS Registry Number.
InChI:InChI=1/C13H15N5/c1-6-5-9-11(17-13(14)18(9)4)12-10(6)15-7(2)8(3)16-12/h5H,1-4H3,(H2,14,17)

146177-58-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5,7,8-tetramethylimidazo[4,5-f]quinoxalin-2-amine

1.2 Other means of identification

Product number -
Other names 5,7,8-Trimethyl-IQX

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:146177-58-4 SDS

146177-58-4Downstream Products

146177-58-4Relevant 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.

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