Cas 83049-75-6,4-Benzyloxy-5-ethyl-2-methyl-4,5-dihydro-oxazole-4-carboxylic acid tert-butyl ester

83049-75-6

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Basic information

Product Name: 4-Benzyloxy-5-ethyl-2-methyl-4,5-dihydro-oxazole-4-carboxylic acid tert-butyl ester
Synonyms: 4-Benzyloxy-5-ethyl-2-methyl-4,5-dihydro-oxazole-4-carboxylic acid tert-butyl ester
CAS NO:83049-75-6
Molecular Formula:
Molecular Weight: 319.401
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: 4-Benzyloxy-5-ethyl-2-methyl-4,5-dihydro-oxazole-4-carboxylic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 4-Benzyloxy-5-ethyl-2-methyl-4,5-dihydro-oxazole-4-carboxylic acid tert-butyl ester(83049-75-6)
EPA Substance Registry System: 4-Benzyloxy-5-ethyl-2-methyl-4,5-dihydro-oxazole-4-carboxylic acid tert-butyl ester(83049-75-6)

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: 83049-75-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 83049-75-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,0,4 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 83049-75:
(7*8)+(6*3)+(5*0)+(4*4)+(3*9)+(2*7)+(1*5)=136
136 % 10 = 6
So 83049-75-6 is a valid CAS Registry Number.

83049-75-6Upstream product

83049-75-6Downstream Products

83049-75-6Relevant academic research and scientific papers

FACILE SYNTHESIS OF ALKOXYOXAZOLINE-CARBOXYLATE FROM 2-(N-BROMOACETYL)AMINO-2-ALKENOATE AND ALCOHOL

Sato, Yoshiaki,Yonezawa, Yasuchika,Shin, Chung-gi

, p. 1463 - 1466 (2007/10/02)

The one-pot reaction of 2-(N-bromoacetyl)amino-2-alkenoate with sodium alkoxide in alcohol proceeded to give 4-alkoxyoxazoline-4-carboxylate.The structure and the formation mechanism were elucidated by the inpendent preparation from 2H-azirine-2-carboxyla

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