Cas 1258005-22-9,tert-butyl (4S)-4-[(1E)-3-{[2-(diphenylphosphoryl)benzoyl]oxy}prop-1-enyl]-2,2-dimethyl-1,3-oxazolidine-3-carboxylate

1258005-22-9

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Basic information

Product Name: tert-butyl (4S)-4-[(1E)-3-{[2-(diphenylphosphoryl)benzoyl]oxy}prop-1-enyl]-2,2-dimethyl-1,3-oxazolidine-3-carboxylate
Synonyms: tert-butyl (4S)-4-[(1E)-3-{[2-(diphenylphosphoryl)benzoyl]oxy}prop-1-enyl]-2,2-dimethyl-1,3-oxazolidine-3-carboxylate
CAS NO:1258005-22-9
Molecular Formula:
Molecular Weight: 561.615
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: tert-butyl (4S)-4-[(1E)-3-{[2-(diphenylphosphoryl)benzoyl]oxy}prop-1-enyl]-2,2-dimethyl-1,3-oxazolidine-3-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl (4S)-4-[(1E)-3-{[2-(diphenylphosphoryl)benzoyl]oxy}prop-1-enyl]-2,2-dimethyl-1,3-oxazolidine-3-carboxylate(1258005-22-9)
EPA Substance Registry System: tert-butyl (4S)-4-[(1E)-3-{[2-(diphenylphosphoryl)benzoyl]oxy}prop-1-enyl]-2,2-dimethyl-1,3-oxazolidine-3-carboxylate(1258005-22-9)

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: 1258005-22-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1258005-22-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,8,0,0 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1258005-22:
(9*1)+(8*2)+(7*5)+(6*8)+(5*0)+(4*0)+(3*5)+(2*2)+(1*2)=129
129 % 10 = 9
So 1258005-22-9 is a valid CAS Registry Number.

1258005-22-9Upstream product

954142-48-4 tert-butyl (4S)-4-[(1E)-3-{[2-(diphenylphosphanyl)benzoyl]oxy}prop-1-enyl]-2,2-dimethyl-1,3-oxazolidine-3-carboxylate

1258005-22-9Downstream Products

1258005-22-9Relevant academic research and scientific papers

1,2-diastereoselective C-C bond-forming reactions for the synthesis of chiral β-branched α-amino acids

Spangenberg, Thomas,Schoenfelder, Angele,Breit, Bernhard,Mann, Andre

experimental part, p. 6005 - 6018 (2011/02/25)

SN2′ sequences have been employed for the synthesis of β-branched α-amino acids using 1,2-diastereocontrol for forming C-C bonds. An oxazolidine fragment derived from Garner's aldehyde provides the handle for facial discrimination and acts as a

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