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561304-48-1

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561304-48-1 Usage

General Description

2-Amino-6-(trifluoromethoxy)benzoic acid is a chemical compound with the molecular formula C8H6F3NO3. It is an aromatic carboxylic acid derivative with a trifluoromethoxy group and an amino group attached to the benzene ring. 2-AMINO-6-(TRIFLUOROMETHOXY)BENZOIC ACID is often used as a building block in organic synthesis and medicinal chemistry. It is also used as a reagent in the synthesis of various pharmaceuticals and agrochemicals. Additionally, this compound has potential applications in the development of new materials and as a tool in biological research.

Check Digit Verification of cas no

The CAS Registry Mumber 561304-48-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,6,1,3,0 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 561304-48:
(8*5)+(7*6)+(6*1)+(5*3)+(4*0)+(3*4)+(2*4)+(1*8)=131
131 % 10 = 1
So 561304-48-1 is a valid CAS Registry Number.
InChI:InChI=1S/C8H6F3NO3/c9-8(10,11)15-5-3-1-2-4(12)6(5)7(13)14/h1-3H,12H2,(H,13,14)

561304-48-1SDS

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 2-Amino-6-(trifluoromethoxy)benzoic acid

1.2 Other means of identification

Product number -
Other names WT080

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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:561304-48-1 SDS

561304-48-1Downstream Products

561304-48-1Relevant articles and documents

Trifluoromethoxy substituted anilines: Metalation as the key step for structural elaboration

Leroux, Frederic,Castagnetti, Eva,Schlosser, Manfred

, p. 4693 - 4699 (2007/10/03)

Trifluoromethoxy-substituted anilines undergo hydrogen/lithium permutation ("metalation") with optional site selectivity depending on the N-protective group employed. N-tert-Butoxycarbonyl-2-and -4-(trifluoromethoxy)aniline react with tert-butyllithium at

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