Cas 184717-01-9,(S)-3-{(2R,3R)-1-Benzyl-2-[(R)-(tert-butyl-dimethyl-silanyloxy)-phenyl-methyl]-4-oxo-azetidin-3-yl}-4-phenyl-oxazolidin-2-one

184717-01-9

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Basic information

Product Name: (S)-3-{(2R,3R)-1-Benzyl-2-[(R)-(tert-butyl-dimethyl-silanyloxy)-phenyl-methyl]-4-oxo-azetidin-3-yl}-4-phenyl-oxazolidin-2-one
Synonyms:
CAS NO:184717-01-9
Molecular Formula:
Molecular Weight: 542.75
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: (S)-3-{(2R,3R)-1-Benzyl-2-[(R)-(tert-butyl-dimethyl-silanyloxy)-phenyl-methyl]-4-oxo-azetidin-3-yl}-4-phenyl-oxazolidin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (S)-3-{(2R,3R)-1-Benzyl-2-[(R)-(tert-butyl-dimethyl-silanyloxy)-phenyl-methyl]-4-oxo-azetidin-3-yl}-4-phenyl-oxazolidin-2-one(184717-01-9)
EPA Substance Registry System: (S)-3-{(2R,3R)-1-Benzyl-2-[(R)-(tert-butyl-dimethyl-silanyloxy)-phenyl-methyl]-4-oxo-azetidin-3-yl}-4-phenyl-oxazolidin-2-one(184717-01-9)

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Safety Statements: N/A
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RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 184717-01-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 184717-01-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,4,7,1 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 184717-01:
(8*1)+(7*8)+(6*4)+(5*7)+(4*1)+(3*7)+(2*0)+(1*1)=149
149 % 10 = 9
So 184717-01-9 is a valid CAS Registry Number.

184717-01-9Upstream product

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184717-01-9Relevant academic research and scientific papers

A study on the asymmetric synthesis of β-lactams through double stereodifferentiating cycloaddition reactions

Palomo, Claudio,Aizpurua, Jesus M.,Mielgo, Antonia,Linden, Anthony

, p. 9186 - 9195 (1996)

The cycloaddition reaction of chiral aminoketenes, generated from their corresponding acid chlorides and triethylamine, with chiral imines is evaluated as the most direct approach for the construction of cis-β-lactams with the absolute stereochemistry at the C3 and C4 positions being controlled by the ketene partner, independently of the absolute stereochemistry of the imine component.

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