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Tyrosine, N-(2,2-dimethyl-1-oxopropyl)-3,5-dimethoxy-O-methyl-b-oxo-, methyl ester is a complex organic compound with the chemical formula C18H25NO6. It is a derivative of the amino acid tyrosine, featuring a methyl ester group, two methoxy groups, and a 2,2-dimethyl-1-oxopropyl group attached to the tyrosine molecule. Tyrosine, N-(2,2-dimethyl-1-oxopropyl)-3,5-dimethoxy-O-methyl-b-oxo-, methyl ester is characterized by its unique structure, which includes a beta-oxo group and an O-methyl group. It is synthesized through a series of chemical reactions and is used in various applications, such as in the pharmaceutical industry for the development of drugs targeting specific enzymes or receptors. The compound's specific properties and potential applications are areas of ongoing research, as its structure offers a foundation for the design of new therapeutic agents.

89205-28-7

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89205-28-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89205-28-7 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, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 89205-28:
(7*8)+(6*9)+(5*2)+(4*0)+(3*5)+(2*2)+(1*8)=147
147 % 10 = 7
So 89205-28-7 is a valid CAS Registry Number.

89205-28-7SDS

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 2-(2,2-Dimethyl-propionylamino)-3-oxo-3-(3,4,5-trimethoxy-phenyl)-propionic acid methyl ester

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

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More Details:89205-28-7 SDS

89205-28-7Relevant 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 (2007/10/02)

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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