Cas 214333-80-9,4-Benzyloxy-2-{(2S,3S)-3-[(R)-1-(tert-butyl-dimethyl-silanyloxy)-ethyl]-4-oxo-azetidin-2-yl}-2-methyl-3-oxo-butyric acid benzyl ester

214333-80-9

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Basic information

Product Name: 4-Benzyloxy-2-{(2S,3S)-3-[(R)-1-(tert-butyl-dimethyl-silanyloxy)-ethyl]-4-oxo-azetidin-2-yl}-2-methyl-3-oxo-butyric acid benzyl ester
Synonyms: 4-Benzyloxy-2-{(2S,3S)-3-[(R)-1-(tert-butyl-dimethyl-silanyloxy)-ethyl]-4-oxo-azetidin-2-yl}-2-methyl-3-oxo-butyric acid benzyl ester
CAS NO:214333-80-9
Molecular Formula:
Molecular Weight: 539.744
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-2-{(2S,3S)-3-[(R)-1-(tert-butyl-dimethyl-silanyloxy)-ethyl]-4-oxo-azetidin-2-yl}-2-methyl-3-oxo-butyric acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 4-Benzyloxy-2-{(2S,3S)-3-[(R)-1-(tert-butyl-dimethyl-silanyloxy)-ethyl]-4-oxo-azetidin-2-yl}-2-methyl-3-oxo-butyric acid benzyl ester(214333-80-9)
EPA Substance Registry System: 4-Benzyloxy-2-{(2S,3S)-3-[(R)-1-(tert-butyl-dimethyl-silanyloxy)-ethyl]-4-oxo-azetidin-2-yl}-2-methyl-3-oxo-butyric acid benzyl ester(214333-80-9)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 214333-80-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 214333-80-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,4,3,3 and 3 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 214333-80:
(8*2)+(7*1)+(6*4)+(5*3)+(4*3)+(3*3)+(2*8)+(1*0)=99
99 % 10 = 9
So 214333-80-9 is a valid CAS Registry Number.

214333-80-9Upstream product

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214333-80-9Relevant academic research and scientific papers

A stereoselective synthesis of a 2-functionalized-methyl-1β-methylcarbapenem key intermediate via decarboxylation

Choi, Woo-Baeg,Lee, Jaemoon,Lynch, Joseph E.,Volante,Reider, Paul J.,Reamer, Robert A.

, p. 1817 - 1818 (1998)

An efficient synthesis of a key intermediate 2a for the synthesis of 2-functionalized methyl-1β-methylcarbapenem antibiotics 1 has been realized via a stereoselective decarboxylation reaction.

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