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Benzoic acid, 5-[2-chloro-6-fluoro-4-(trifluoromethyl)phenoxy]-2-nitro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

80172-08-3

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80172-08-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80172-08-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,1,7 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 80172-08:
(7*8)+(6*0)+(5*1)+(4*7)+(3*2)+(2*0)+(1*8)=103
103 % 10 = 3
So 80172-08-3 is a valid CAS Registry Number.

80172-08-3SDS

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 5-[2-chloro-6-fluoro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoic acid

1.2 Other means of identification

Product number -
Other names 2-Nitro-5-(2-chloro-6-fluoro-4-trifluoromethyl phenoxy)benzoic acid

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:80172-08-3 SDS

80172-08-3Relevant academic research and scientific papers

Preparation of fluorine-containing diphenyl ethers

-

, (2008/06/13)

A method of preparing a diphenyl ether compound of the formula (II) STR1 wherein X is F, Cl or Br; Z is hydrogen, halogen, NO2 of CN; and W is methyl, cyano, CH3 CO--, or a group --C--OR, wherein R is --OH; --OM wherein M is a cation; OR1 wherein R1 is an optionally substituted aliphatic radical; --NR2 R3 wherein R2 and R3 are each hydrogen or an optionally substituted aliphatic radical; or --NHSO2 R4 wherein R4 is alkyl of 1 to 6 carbon atoms, which comprises reacting a 3-X-substituted-4,5-difluorobenzotrifluoride with a salt of a 3,4-W,Z-substituted phenol. The invention further comprises novel 3-X-4,5-difluorobenzotrifluorides for use in the process.

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