Cas 1269630-01-4,(2S,5S,1'S)-5-[1'-(4-bromophenyl)-1'-hydroxymethyl]-2-(tert-butyl)-5-phenyl-1,3-dioxolan-4-one

1269630-01-4

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Basic information

Product Name: (2S,5S,1'S)-5-[1'-(4-bromophenyl)-1'-hydroxymethyl]-2-(tert-butyl)-5-phenyl-1,3-dioxolan-4-one
Synonyms: (2S,5S,1'S)-5-[1'-(4-bromophenyl)-1'-hydroxymethyl]-2-(tert-butyl)-5-phenyl-1,3-dioxolan-4-one
CAS NO:1269630-01-4
Molecular Formula:
Molecular Weight: 405.288
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: (2S,5S,1'S)-5-[1'-(4-bromophenyl)-1'-hydroxymethyl]-2-(tert-butyl)-5-phenyl-1,3-dioxolan-4-one(CAS DataBase Reference)
NIST Chemistry Reference: (2S,5S,1'S)-5-[1'-(4-bromophenyl)-1'-hydroxymethyl]-2-(tert-butyl)-5-phenyl-1,3-dioxolan-4-one(1269630-01-4)
EPA Substance Registry System: (2S,5S,1'S)-5-[1'-(4-bromophenyl)-1'-hydroxymethyl]-2-(tert-butyl)-5-phenyl-1,3-dioxolan-4-one(1269630-01-4)

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: 1269630-01-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1269630-01-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,9,6,3 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1269630-01:
(9*1)+(8*2)+(7*6)+(6*9)+(5*6)+(4*3)+(3*0)+(2*0)+(1*1)=164
164 % 10 = 4
So 1269630-01-4 is a valid CAS Registry Number.

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1269630-01-4Relevant academic research and scientific papers

(S)-Mandelic acid enolate as a chiral benzoyl anion equivalent for the enantioselective synthesis of non-symmetrically substituted benzoins

Blay, Gonzalo,Fernández, Isabel,Monje, Belén,Montesinos-Magraner, Marc,Pedro, José R.

experimental part, p. 881 - 890 (2011/03/19)

A strategy for the enantioselective synthesis of non-symmetrically substituted benzoins from (S)-mandelic acid and aromatic aldehydes has been developed. This strategy is based on a diastereoselective aldol reaction of the lithium enolate of the 1,3-dioxo

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