Cas 138235-06-0,(2S,3S)-3-[(R)-1-(tert-Butyl-diphenyl-silanyl)-ethyl]-1-(4-methoxy-phenyl)-4-oxo-azetidine-2-carboxylic acid methyl ester

138235-06-0

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Basic information

Product Name: (2S,3S)-3-[(R)-1-(tert-Butyl-diphenyl-silanyl)-ethyl]-1-(4-methoxy-phenyl)-4-oxo-azetidine-2-carboxylic acid methyl ester
Synonyms:
CAS NO:138235-06-0
Molecular Formula:
Molecular Weight: 501.698
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: (2S,3S)-3-[(R)-1-(tert-Butyl-diphenyl-silanyl)-ethyl]-1-(4-methoxy-phenyl)-4-oxo-azetidine-2-carboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3S)-3-[(R)-1-(tert-Butyl-diphenyl-silanyl)-ethyl]-1-(4-methoxy-phenyl)-4-oxo-azetidine-2-carboxylic acid methyl ester(138235-06-0)
EPA Substance Registry System: (2S,3S)-3-[(R)-1-(tert-Butyl-diphenyl-silanyl)-ethyl]-1-(4-methoxy-phenyl)-4-oxo-azetidine-2-carboxylic acid methyl ester(138235-06-0)

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: 138235-06-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 138235-06-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,2,3 and 5 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 138235-06:
(8*1)+(7*3)+(6*8)+(5*2)+(4*3)+(3*5)+(2*0)+(1*6)=120
120 % 10 = 0
So 138235-06-0 is a valid CAS Registry Number.

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138235-06-0Relevant academic research and scientific papers

Formation of 3-azetidin-2-ones: Stereocontrolled Formal Approach to (+/-)-Thienamycin and (+/-)-β-(Hydroxyalkyl)aspartic Acid Derivatives

Palomo, Claudio,Aizpurua, Jesus M.,Urchegui, Raquel,Iturburu, Miren

, p. 1571 - 1579 (2007/10/02)

Reaction between (+/-)-β-(dimethylphenylsilyl)alkanoyl chlorides and imines of glyoxylic esters provided a route to (+/-)-cis-3--4-alkoxycarbonyl β-lactams, while addition of the Fleming's silylcuprate reagent to methyl crot

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