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Ethyl 2-[(2-hydroxybenzoyl)amino]acetate is a chemical compound with the molecular formula C12H13NO4. It is an organic ester derived from 2-aminobutyric acid and 2-hydroxybenzoic acid, featuring a hydroxyl group attached to the benzene ring. ethyl 2-[(2-hydroxybenzoyl)amino]acetate is known for its potential applications in pharmaceuticals and as an intermediate in the synthesis of various drugs and chemical products. It is characterized by its ability to form salts and has been studied for its potential therapeutic properties. The compound's structure and reactivity make it a valuable component in the development of new chemical entities, particularly in the field of medicinal chemistry.

5853-89-4

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5853-89-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5853-89-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,5 and 3 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5853-89:
(6*5)+(5*8)+(4*5)+(3*3)+(2*8)+(1*9)=124
124 % 10 = 4
So 5853-89-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H13NO4/c1-2-16-10(14)7-12-11(15)8-5-3-4-6-9(8)13/h3-6,13H,2,7H2,1H3,(H,12,15)

5853-89-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-[(2-hydroxybenzoyl)amino]acetate

1.2 Other means of identification

Product number -
Other names N-(2-hydroxy-benzoyl)-glycine ethyl 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 -
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More Details:5853-89-4 SDS

5853-89-4Downstream Products

5853-89-4Relevant academic research and scientific papers

PHOTOREACTIONS OF 4- AND 3-AZIDOCOUMARINS IN THE PRESENCE OF NUCLEOPHILES

Ito, Keiichi,Higuchi, Yukako,Tame, Chika,Hariya, Junko

, p. 937 - 947 (2007/10/02)

The photoreactions of 4-azidocoumarins (1) and 3-azidocoumarin (2) in the presence of nucleophiles such as alcohols, thiol or amines generally gave 4-substituted 3-amino- and/or 3-substituted 4-aminocoumarins, while pyrone ring fission with incorporation of two moles of nucleophile was observed in the reaction of 1 in the presence of primary or secondary aliphatic amine as a nucleophile.Plausible mechanisms for these reactions are suggested.

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