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Benzoic acid, 3-[(2-methoxy-2-oxoethyl)amino]-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

651749-29-0

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651749-29-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 651749-29-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,1,7,4 and 9 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 651749-29:
(8*6)+(7*5)+(6*1)+(5*7)+(4*4)+(3*9)+(2*2)+(1*9)=180
180 % 10 = 0
So 651749-29-0 is a valid CAS Registry Number.

651749-29-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-[(2-methoxy-2-oxoethyl)amino]benzoate

1.2 Other means of identification

Product number -
Other names 3-(Methoxycarbonylmethyl-amino)-benzoic acid methyl ester

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:651749-29-0 SDS

651749-29-0Relevant academic research and scientific papers

Synthesis of some n-aryl α-Amino acids using diaryliodonium salts

Mckerrow, Jason D.,Al-Rawi, Jasim M.,Brooks, Peter

experimental part, p. 1227 - 1236 (2012/09/22)

Bis[(3'-methoxycarbonyl)phenyl]iodonium bromide (4a), bis (4'-methoxyphenyl)iodonium iodide (4b) and bis (4'-acetamidophenyl)iodonium iodide (4c) were employed for the first time in the arylation of α-amino acid methyl esters. Yields of the synthesised products 5, 6 and 7 were good to high. These were then hydrolyzed to the corresponding N-aryl α-amino acids 8 and 9. The chiral integrity of the amino acids was maintained throughout the reaction sequence as confirmed by the synthesis of chiral tripeptide 10 and dipeptides 11. The structures of the new compounds were confirmed by IR, 1H and 13C NMR in addition to CHN microanalysis or high resolution mass spectrometry.

Ureido substituted benzoic acid compounds and their use for nonsense suppression and the treatment of disease

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Page/Page column 49, (2008/06/13)

The invention encompasses ureido substituted benzoic acid compounds, compositions comprising the compounds and methods for treating or preventing diseases associated with nonsense mutations of mRNA by administering these compounds or compositions.

UREIDO SUBSTITUTED BENZOIC ACID COMPOUNDS AND THEIR USE FOR NONSENSE SUPPRESSION AND THE TREATMENT OF DISEASE

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Page 91-92, (2010/02/06)

The invention encompasses ureido substituted benzoic acid compounds, compositions comprising the compounds and methods for treating or preventing diseases associated with nonsense mutations of mRNA by administering these compounds or compositions.

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