Cas 175656-24-3,(S)-3-{(2R,3R)-2-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-3-ethyl-5-trimethylsilanyl-pent-4-ynoyl}-4-isopropyl-oxazolidin-2-one

175656-24-3

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Basic information

Product Name: (S)-3-{(2R,3R)-2-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-3-ethyl-5-trimethylsilanyl-pent-4-ynoyl}-4-isopropyl-oxazolidin-2-one
Synonyms: (S)-3-{(2R,3R)-2-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-3-ethyl-5-trimethylsilanyl-pent-4-ynoyl}-4-isopropyl-oxazolidin-2-one
CAS NO:175656-24-3
Molecular Formula:
Molecular Weight: 591.938
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)-2-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-3-ethyl-5-trimethylsilanyl-pent-4-ynoyl}-4-isopropyl-oxazolidin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (S)-3-{(2R,3R)-2-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-3-ethyl-5-trimethylsilanyl-pent-4-ynoyl}-4-isopropyl-oxazolidin-2-one(175656-24-3)
EPA Substance Registry System: (S)-3-{(2R,3R)-2-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-3-ethyl-5-trimethylsilanyl-pent-4-ynoyl}-4-isopropyl-oxazolidin-2-one(175656-24-3)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 175656-24-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 175656-24-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,6,5 and 6 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 175656-24:
(8*1)+(7*7)+(6*5)+(5*6)+(4*5)+(3*6)+(2*2)+(1*4)=163
163 % 10 = 3
So 175656-24-3 is a valid CAS Registry Number.

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175656-24-3Relevant academic research and scientific papers

Formal total syntheses of the β-lactam antibiotics thienamycin and PS-5

Jacobi, Peter A.,Murphree, Shaun,Rupprecht, Frederic,Zheng, Wanjun

, p. 2413 - 2427 (1996)

Chiral nonracemic acetylenic acids of general structure 11, prepared using the Schreiber modification of the Nicholas reaction, have been converted to β-amino acid derivatives of type 12 by a two-step sequence involving Curtius rearrangement followed by o

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