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141940-29-6

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141940-29-6 Usage

General Description

N-BOC-5-trifluoromethylanthranilic acid is a chemical compound that belongs to the class of anthranilic acids. It is commonly used as a building block in organic synthesis, specifically in the synthesis of pharmaceutical compounds. The "N-BOC" in its name refers to the tert-butoxycarbonyl protective group attached to the nitrogen atom, which helps to control the reactivity of the molecule. The trifluoromethyl group attached to the aromatic ring makes this compound useful in medicinal chemistry for the development of drugs with improved pharmacokinetic properties. Overall, N-BOC-5-trifluoromethylanthranilic acid is a versatile chemical with uses in drug discovery and organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 141940-29-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,9,4 and 0 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 141940-29:
(8*1)+(7*4)+(6*1)+(5*9)+(4*4)+(3*0)+(2*2)+(1*9)=116
116 % 10 = 6
So 141940-29-6 is a valid CAS Registry Number.

141940-29-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(2-methylpropan-2-yl)oxycarbonylamino]-5-(trifluoromethyl)benzoic acid

1.2 Other means of identification

Product number -
Other names 2-({[(1,1-dimethylethyl)oxy]carbonyl}amino)-5-(trifluoromethyl)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:141940-29-6 SDS

141940-29-6Relevant articles and documents

AZABIPHENYLAMINOBENZOIC ACID DERIVATIVES AS DHODH INHIBITORS

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, (2009/04/25)

New azabiphenylaminobenzoic acid derivatives having the chemcial structure of formula (I) are disclosed; as well as process for their preparation, pharmaceutical compositions comprising them and their use in therapy as inhibitors of the dehydroorotate dihydrogenase (DHODH)

Bacterial translation inhibitors, 1-acylindazol-3-ols as anthranilic acid mimics

Stiff, Cory,Graber, David R.,Thorarensen, Atli,Wakefield, Brian D.,Marotti, Keith R.,Melchior, Earline P.,Sweeney, Michael T.,Han, Fusen,Rohrer, Douglas C.,Zurenko, Gary E.,Romero, Donna L.

scheme or table, p. 6293 - 6297 (2009/07/18)

The discovery and initial optimization of a novel anthranilic acid derived class of antibacterial agents has been described in a recent series of papers. This paper describes the discovery of 1-acylindazol-3-ols as a novel bioisostere of an anthranilic acid. The synthesis and structure-activity relationships of the indazol bioisosteres are described herein.

SUBSTITUTED AMINO PHENYLACETIC ACIDS, DERIVATIVES THEREOF, THEIR PREPARATION AND THEIR USE AS CYCLOOXYGENASE 2 (COX-2) INHIBITORS

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Page 53-55, (2008/06/13)

Compounds of formula (I) wherein R is hydrogen, lower alkyl, (C3-C8)cycloalkyl, hydroxy, halo, lower alkoxy, trifluoromethoxy, trifluoromethyl or cyano; and A is biaryl, optionally substituted β-naphthyl, bicyclic heterocyclic aryl, (C3-C6)cycloalkylmonocyclic carbocyclic aryl, or (C5 or C6)cycloalkane fused-monocyclic carbocyclic aryl; pharmaceutically acceptable salts thereof, and pharmaceutically acceptable esters thereof; which are useful for the treatment of COX-2 dependent disorders.

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