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143309-87-9

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143309-87-9 Usage

General Description

6,7-Dichloro-2-methyl-3-(trifluoromethyl)quinoxaline is a chemical compound with the molecular formula C9H5Cl2F3N2. It is a quinoxaline derivative that is commonly used in the pharmaceutical and agrochemical industries. 6,7-Dichloro-2-methyl-3-(trifluoromethyl)quinoxaline is known for its potent antimicrobial and antiparasitic properties, and it has gained attention for its potential use in the development of new drugs and pesticides. It is a white to off-white solid that is soluble in organic solvents and has a relatively high melting point. 6,7-Dichloro-2-methyl-3-(trifluoromethyl)quinoxaline is considered to be a valuable building block for the synthesis of various bioactive compounds due to its unique structure and versatile reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 143309-87-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,3,0 and 9 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 143309-87:
(8*1)+(7*4)+(6*3)+(5*3)+(4*0)+(3*9)+(2*8)+(1*7)=119
119 % 10 = 9
So 143309-87-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H5Cl2F3N2/c1-4-9(10(13,14)15)17-8-3-6(12)5(11)2-7(8)16-4/h2-3H,1H3

143309-87-9SDS

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 6,7-Dichloro-2-methyl-3-(trifluoromethyl)quinoxaline

1.2 Other means of identification

Product number -
Other names 6,7-Dichloro-2-methyl-3-trifluoromethylquinoxaline

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:143309-87-9 SDS

143309-87-9Downstream Products

143309-87-9Relevant articles and documents

19F NMR Studies on the Mechanism of Riboflavin Synthase. Synthesis of 6-(Trifluoromethyl)-7-oxo-8-(D-ribityl)lumazine and 6-(trifluoromethyl)-7-methyl-8-(D-ribityl)lumazine

Cushman, Mark,Patel, Hemantkumar H.,Scheuring, Johannes,Bacher, Adelbert

, p. 5630 - 5643 (2007/10/02)

The reactions of hexafluoropropene oxide (19), methyl trifluoropyruvate (21), and 1,1,1-trifluorobutane-2,3-dione (45) with a series of ortho diamines were investigated as an approach to the synthesis of trifluoromethyl-substituted quinoxalinones and luma

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