Cas 169059-62-5,2-((S)-1-Benzyloxycarbonylamino-2-methylcarbamoyl-ethyl)-5-methyl-thiazole-4-carboxylic acid ethyl ester

169059-62-5

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Basic information

Product Name: 2-((S)-1-Benzyloxycarbonylamino-2-methylcarbamoyl-ethyl)-5-methyl-thiazole-4-carboxylic acid ethyl ester
Synonyms:
CAS NO:169059-62-5
Molecular Formula:
Molecular Weight: 405.475
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: 2-((S)-1-Benzyloxycarbonylamino-2-methylcarbamoyl-ethyl)-5-methyl-thiazole-4-carboxylic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-((S)-1-Benzyloxycarbonylamino-2-methylcarbamoyl-ethyl)-5-methyl-thiazole-4-carboxylic acid ethyl ester(169059-62-5)
EPA Substance Registry System: 2-((S)-1-Benzyloxycarbonylamino-2-methylcarbamoyl-ethyl)-5-methyl-thiazole-4-carboxylic acid ethyl ester(169059-62-5)

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: 169059-62-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 169059-62-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,0,5 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 169059-62:
(8*1)+(7*6)+(6*9)+(5*0)+(4*5)+(3*9)+(2*6)+(1*2)=165
165 % 10 = 5
So 169059-62-5 is a valid CAS Registry Number.

169059-62-5Upstream product

593-51-1 methylamine hydrochloride

169059-62-5Downstream Products

169059-62-5Relevant academic research and scientific papers

Degradation studies of antibiotic MDL 62,879 (GE2270A) and revision of the structure

Tavecchia,Gentili,Kurz,Sottani,Bonfichi,Selva,Lociuro,Restelli,Ciabatti

, p. 4867 - 4890 (1995)

Fragments of the thiopeptide antibiotic MDL 62,879 (GE2270A) were prepared under mild degradation conditions. Their structures were determined by spectroscopic techniques and by comparison to synthetic reference thiazolyl dipeptides. The two thiazolyl ami

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