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Tyrosine, N-benzoyl-3,5-dimethoxy-O-methyl-b-oxo-, methyl ester is a complex organic compound with the chemical formula C19H21NO6. It is derived from the amino acid tyrosine and features a benzoyl group, two methoxy groups, and a methyl ester group attached to the tyrosine backbone. Tyrosine, N-benzoyl-3,5-dimethoxy-O-methyl-b-oxo-, methyl ester is characterized by its unique structure, which includes a beta-oxo group (a carbonyl group adjacent to a carbon-carbon double bond) and an O-methyl group, which is a methyl group attached to an oxygen atom. The compound is synthesized through a series of chemical reactions and is used in various applications, such as in the synthesis of pharmaceuticals and as a research tool in the study of tyrosine-derived compounds. Its specific properties and potential applications are of interest to chemists and researchers in the field of organic chemistry and drug development.

89205-30-1

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89205-30-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89205-30-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,2,0 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 89205-30:
(7*8)+(6*9)+(5*2)+(4*0)+(3*5)+(2*3)+(1*0)=141
141 % 10 = 1
So 89205-30-1 is a valid CAS Registry Number.

89205-30-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-benzamido-3-oxo-3-(3,4,5-trimethoxyphenyl)propanoate

1.2 Other means of identification

Product number -
Other names -

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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More Details:89205-30-1 SDS

89205-30-1Relevant academic research and scientific papers

Syntheses of 5-substituted oxazole-4-carboxylic acid derivatives with inhibitory activity on blood platelet aggregation

Ozaki,Maeda,Iwasaki,Matsumoto,Odawara,Sasaki,Morita

, p. 4417 - 4424 (1983)

Methyl 5-substituted oxazole-4-carboxylates were synthesized by the reaction of methyl α-isocyanoacetate with acylating reagents in the presence of bases. The oxazole methyl esters were converted into the carboxylic acids and the carboxamides. Then, N-alk

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