Cas 1013088-41-9,(2'S,4S)-3-(2-fluoro-3-cyclohexyl-1-oxopropyl)-4-phenylmethyl-2-oxazolidinone

1013088-41-9

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Basic information

Product Name: (2'S,4S)-3-(2-fluoro-3-cyclohexyl-1-oxopropyl)-4-phenylmethyl-2-oxazolidinone
Synonyms: (2'S,4S)-3-(2-fluoro-3-cyclohexyl-1-oxopropyl)-4-phenylmethyl-2-oxazolidinone
CAS NO:1013088-41-9
Molecular Formula:
Molecular Weight: 333.403
EINECS: N/A
Product Categories: N/A
Mol File: 1013088-41-9.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: (2'S,4S)-3-(2-fluoro-3-cyclohexyl-1-oxopropyl)-4-phenylmethyl-2-oxazolidinone(CAS DataBase Reference)
NIST Chemistry Reference: (2'S,4S)-3-(2-fluoro-3-cyclohexyl-1-oxopropyl)-4-phenylmethyl-2-oxazolidinone(1013088-41-9)
EPA Substance Registry System: (2'S,4S)-3-(2-fluoro-3-cyclohexyl-1-oxopropyl)-4-phenylmethyl-2-oxazolidinone(1013088-41-9)

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: 1013088-41-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1013088-41-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,3,0,8 and 8 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1013088-41:
(9*1)+(8*0)+(7*1)+(6*3)+(5*0)+(4*8)+(3*8)+(2*4)+(1*1)=99
99 % 10 = 9
So 1013088-41-9 is a valid CAS Registry Number.

1013088-41-9Upstream product

136187-43-4 (4S)-3-(3-cyclohexyl-1-oxopropyl)-4-phenylmethyl-2-oxazolidinone

1013088-41-9Downstream Products

1013088-41-9Relevant articles and documents

Enantioselective synthesis of α-fluorinated β2-amino acids

Edmonds, Michael K.,Graichen, Florian H.M.,Gardiner, James,Abell, Andrew D.

, p. 885 - 887 (2008)

A methodology for the enantioselective synthesis of α-fluorinated β2-amino acids has been developed from readily available carboxylic acids 3. Conversion to the Evan's oxazolidinone followed by enantioselective fluorination and alkylation gave 7 in high diastereomeric excess (>95%). Subsequent removal of the oxazolidinone and amination at the Bn-protected hydroxyl center gave optically active α-fluorinated β2-amino acids.

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