Cas 175880-80-5,[(3S,4R)-3-[(R)-1-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-2-oxo-4-((S)-2-oxo-cyclopentyl)-azetidin-1-yl]-(triphenyl-λ<sup>5</sup>-phosphanylidene)-acetic acid allyl ester

175880-80-5

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Basic information

Product Name: [(3S,4R)-3-[(R)-1-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-2-oxo-4-((S)-2-oxo-cyclopentyl)-azetidin-1-yl]-(triphenyl-λ⁵-phosphanylidene)-acetic acid allyl ester
Synonyms:
CAS NO:175880-80-5
Molecular Formula:
Molecular Weight: 669.873
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: [(3S,4R)-3-[(R)-1-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-2-oxo-4-((S)-2-oxo-cyclopentyl)-azetidin-1-yl]-(triphenyl-λ⁵-phosphanylidene)-acetic acid allyl ester(CAS DataBase Reference)
NIST Chemistry Reference: [(3S,4R)-3-[(R)-1-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-2-oxo-4-((S)-2-oxo-cyclopentyl)-azetidin-1-yl]-(triphenyl-λ⁵-phosphanylidene)-acetic acid allyl ester(175880-80-5)
EPA Substance Registry System: [(3S,4R)-3-[(R)-1-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-2-oxo-4-((S)-2-oxo-cyclopentyl)-azetidin-1-yl]-(triphenyl-λ⁵-phosphanylidene)-acetic acid allyl ester(175880-80-5)

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: 175880-80-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 175880-80-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,8,8 and 0 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 175880-80:
(8*1)+(7*7)+(6*5)+(5*8)+(4*8)+(3*0)+(2*8)+(1*0)=175
175 % 10 = 5
So 175880-80-5 is a valid CAS Registry Number.

175880-80-5Upstream product

175880-80-5Downstream Products

175880-80-5Relevant academic research and scientific papers

Synthesis and biological activity of novel tricyclic β-lactams

Biondi, Stefano,Gaviraghi, Giovanni,Rossi, Tino

, p. 525 - 528 (1996)

The synthesis of the preliminary data on microbiological activity of some tricyclic β-lactam derivatives (4), analogues of synthetic 'trinems', is described. Compound 14, key intermediate in the synthesis of 18, was stereoselectively obtained from its unsubstituted analogue, 12B, in 4 steps through enolphosphate 13.

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