Cas 127118-32-5,(S)-3-{(2S,3R)-2-Bromo-3-hydroxy-3-[2-(8-phenyl-octyl)-phenyl]-propionyl}-4-isopropyl-oxazolidin-2-one

127118-32-5

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Basic information

Product Name: (S)-3-{(2S,3R)-2-Bromo-3-hydroxy-3-[2-(8-phenyl-octyl)-phenyl]-propionyl}-4-isopropyl-oxazolidin-2-one
Synonyms:
CAS NO:127118-32-5
Molecular Formula:
Molecular Weight: 544.529
EINECS: N/A
Product Categories: N/A
Mol File: 127118-32-5.mol
Article Data: 1

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-{(2S,3R)-2-Bromo-3-hydroxy-3-[2-(8-phenyl-octyl)-phenyl]-propionyl}-4-isopropyl-oxazolidin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (S)-3-{(2S,3R)-2-Bromo-3-hydroxy-3-[2-(8-phenyl-octyl)-phenyl]-propionyl}-4-isopropyl-oxazolidin-2-one(127118-32-5)
EPA Substance Registry System: (S)-3-{(2S,3R)-2-Bromo-3-hydroxy-3-[2-(8-phenyl-octyl)-phenyl]-propionyl}-4-isopropyl-oxazolidin-2-one(127118-32-5)

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: 127118-32-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 127118-32-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,1,1 and 8 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 127118-32:
(8*1)+(7*2)+(6*7)+(5*1)+(4*1)+(3*8)+(2*3)+(1*2)=105
105 % 10 = 5
So 127118-32-5 is a valid CAS Registry Number.

127118-32-5Upstream product

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127118-32-5Relevant articles and documents

A PREDOMINATELY ANTI-STEREOSELECTIVE CHIRAL METAL DIRECTED ALDOL CONDENSATION WITH AROMATIC ALDEHYDES

Pridgen, Lendon N.,Abdel-Magid, A.,Lantos, I.

, p. 5539 - 5542 (2007/10/02)

Chiral haloacetyl oxazolidinones were reacted with aromatic aldehydes via their kinetically generated Z-enolates to yield predominately anti aldol adducts.The reaction is postulated to proceed thru a boat-like transition state.A unique reversal of chirality was observed in using stannous enolates.

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