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Tyrosine, N-acetyl-3,5-dimethoxy-O-methyl-b-oxo-, methyl ester is a complex organic compound with the chemical formula C14H19NO6. It is derived from the amino acid tyrosine and is characterized by the presence of an N-acetyl group, two methoxy groups at the 3rd and 5th positions, and a methyl ester group. Tyrosine, N-acetyl-3,5-dimethoxy-O-methyl-b-oxo-, methyl ester is a synthetic derivative of tyrosine and is not commonly found in nature. It is used in various chemical and pharmaceutical applications, such as the synthesis of other complex molecules and as an intermediate in the production of certain drugs. Due to its specific structure, it may have potential therapeutic properties, although further research is needed to explore its full potential.

89205-26-5

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89205-26-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89205-26-5 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 6 respectively.
Calculate Digit Verification of CAS Registry Number 89205-26:
(7*8)+(6*9)+(5*2)+(4*0)+(3*5)+(2*2)+(1*6)=145
145 % 10 = 5
So 89205-26-5 is a valid CAS Registry Number.

89205-26-5SDS

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 N-acetyl-3,5-dimethoxy-O-methyl-β-oxotyrosinate

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:89205-26-5 SDS

89205-26-5Relevant 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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