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(4-TERT-BUTYL-BENZOYLAMINO)-ACETIC ACID is a chemical compound with the molecular formula C14H19NO3. It is an amide derivative of acetic acid, containing a tert-butyl group and a benzoylamino group. (4-TERT-BUTYL-BENZOYLAMINO)-ACETIC ACID is of interest to chemists and pharmaceutical researchers due to its potential applications in the development of new medications and bioactive compounds.
Used in Pharmaceutical Research and Drug Development:
(4-TERT-BUTYL-BENZOYLAMINO)-ACETIC ACID is used as a building block for the synthesis of various pharmaceutical compounds. Its unique structure allows for the creation of diverse molecules with potential therapeutic properties.
Used in Organic Synthesis:
(4-TERT-BUTYL-BENZOYLAMINO)-ACETIC ACID is used as a reagent in organic synthesis, particularly in the preparation of complex organic compounds. Its versatility in chemical reactions makes it a valuable tool for chemists working on the development of new chemical entities.

87015-91-6

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87015-91-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87015-91-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,0,1 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 87015-91:
(7*8)+(6*7)+(5*0)+(4*1)+(3*5)+(2*9)+(1*1)=136
136 % 10 = 6
So 87015-91-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H17NO3/c1-13(2,3)10-6-4-9(5-7-10)12(17)14-8-11(15)16/h4-7H,8H2,1-3H3,(H,14,17)(H,15,16)

87015-91-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-TERT-BUTYL-BENZOYLAMINO)-ACETIC ACID

1.2 Other means of identification

Product number -
Other names N-[4-(1,1-dimethylethyl)benzoyl]-glycine

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:87015-91-6 SDS

87015-91-6Relevant academic research and scientific papers

NOVEL COMPOUND AND COMPOSITION FOR PREVENTION OR TREATMENT OF RESPIRATORY DISEASES COMPRISING SAME AS ACTIVE INGREDIENT

-

, (2022/02/19)

The present invention relates to a novel compound, and a composition for preventing or treating of respiratory disease comprising the novel compound, E- or Z-isomer thereof, optical isomer thereof, a mixture of two isomers thereof, precursor thereof, pharmaceutically acceptable salt thereof or solvate thereof as an active ingredient.

Palladium-catalyzed ortho-arylation of benzoic acid derivatives via C-H bond activation using an aminoacetic acid bidentate directing group

Zhou, Xiaomeng,Wang, Qing,Zhao, Weihua,Xu, Songsong,Zhang, Wei,Chen, Junmin

supporting information, p. 851 - 855 (2015/01/30)

A highly efficient protocol for the palladium-catalyzed ortho-arylation of benzoic acid derivatives by aryl iodides is described with an aminoacetic acid based N,O bidentate directing group. This protocol can be applied to various benzoyl aminoacetic acids and aryl iodides with both electron-donating and electron-withdrawing groups. Remarkably, the nature of a new directing group drives selective C-H bond activation to afford only monoarylation products in good to excellent yields.

A convenient method for synthesis of 5-chloro-2-aryloxazole-4-carbaldehyde with vilsmeier reagent

Jin, Can,Chen, Jun,Su, Weike

experimental part, p. 153 - 161 (2011/04/21)

A convenient method for synthesis of 5-chloro-2-aryloxazole-4-carbaldehyde 3 in moderate to good yields had been developed via the Vilsmeier reaction of readily available N-arylglycine 2 at 100 °C, provided a novel route for the construction of nitrogen heterocycles. A series of these compounds were synthesized by this method and optimization of conditions was performed. The Japan Institute of Heterocyclic Chemistry.

2-SUBSTITUTED-3-PROPENAMIDE DERIVATIVES AND METHODS OF USING THE SAME

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Page 57, (2010/02/07)

This invention provides 2-substituted-propenamide derivatives and their compositions for the treament of hepatitis B virus and/or hepatitis D virus.

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