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119385-80-7

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119385-80-7 Usage

Uses

3-Amino-2,4,5-trifluorobenzoic Acid is used in the preparation of 7-(azaspiroalkanyl)quinolonecarboxylates and analogs as bactericides.

Check Digit Verification of cas no

The CAS Registry Mumber 119385-80-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,3,8 and 5 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 119385-80:
(8*1)+(7*1)+(6*9)+(5*3)+(4*8)+(3*5)+(2*8)+(1*0)=147
147 % 10 = 7
So 119385-80-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H4F3NO2/c8-3-1-2(7(12)13)4(9)6(11)5(3)10/h1H,11H2,(H,12,13)

119385-80-7SDS

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-AMINO-2,4,5-TRIFLUOROBENZOIC ACID

1.2 Other means of identification

Product number -
Other names PC1099G

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:119385-80-7 SDS

119385-80-7Relevant articles and documents

Preparation method of 3-chloro-2,4,5-trifluorobenzoic acid

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Paragraph 5; 6, (2019/12/29)

The invention discloses a preparation method of 3-chloro-2,4,5-trifluorobenzoic acid. The reaction equation of the method is shown in the description. The preparation method concretely comprises the following steps: preparing a compound of formula (1) fro

Process for the synthesis of 3-chloro-2,4,5-trifluorobenzoic acid

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, (2008/06/13)

An improved process for the preparation of 3-chloro-2,4,5-trifluorobenzoic acid is described which involves reaction of a diester of 3,4,5,6-tetrafluoro-1,2-benzenedicarboxylic acid with a substituted amine to afford 3-amino-2,4,5-trifluorobenzoic acid followed by subsequent conversion of the amio intermediate into 3-chloro-2,4,5-trifluorobenzoic acid.

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