Cas 1393377-83-7,methyl (R)-2-((S)-1-(tert-butyldiphenylsilyloxy)ethyl)-4,5-dihydrothiazole-4-carboxylate

1393377-83-7

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Basic information

Product Name: methyl (R)-2-((S)-1-(tert-butyldiphenylsilyloxy)ethyl)-4,5-dihydrothiazole-4-carboxylate
Synonyms:
CAS NO:1393377-83-7
Molecular Formula:
Molecular Weight: 427.64
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: methyl (R)-2-((S)-1-(tert-butyldiphenylsilyloxy)ethyl)-4,5-dihydrothiazole-4-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: methyl (R)-2-((S)-1-(tert-butyldiphenylsilyloxy)ethyl)-4,5-dihydrothiazole-4-carboxylate(1393377-83-7)
EPA Substance Registry System: methyl (R)-2-((S)-1-(tert-butyldiphenylsilyloxy)ethyl)-4,5-dihydrothiazole-4-carboxylate(1393377-83-7)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1393377-83-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1393377-83-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,3,3,7 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1393377-83:
(9*1)+(8*3)+(7*9)+(6*3)+(5*3)+(4*7)+(3*7)+(2*8)+(1*3)=197
197 % 10 = 7
So 1393377-83-7 is a valid CAS Registry Number.

1393377-83-7Upstream product

125941-75-5 (S)-2-[(1,1-dimethylethyl)diphenylsilyl]oxypropanoic acid

1393377-83-7Downstream Products

1393377-83-7Relevant academic research and scientific papers

Concise synthesis of 2,4-disubstituted thiazoles from β-azido disulfides and carboxylic acids or anhydrides: Asymmetric synthesis of cystothiazole C

Liu, Yi,Sun, Xue,Zhang, Xing,Liu, Jun,Du, Yuguo

, p. 8453 - 8461 (2014/12/10)

A novel and efficient method for the one-pot synthesis of 2,4-disubstituted thiazoles from carboxylic acids or anhydrides is presented. Based on this new method, the total synthesis of the bis-2,4-disubstituted bis(thiazoles) natural product cystothiazole C is also presented. This journal is

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