Cas 632332-46-8,Acrylic acid (1S,2R)-1-benzyloxymethyl-2-(tert-butyl-diphenyl-silanyloxymethyl)-but-3-enyl ester

632332-46-8

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Basic information

Product Name: Acrylic acid (1S,2R)-1-benzyloxymethyl-2-(tert-butyl-diphenyl-silanyloxymethyl)-but-3-enyl ester
Synonyms: Acrylic acid (1S,2R)-1-benzyloxymethyl-2-(tert-butyl-diphenyl-silanyloxymethyl)-but-3-enyl ester
CAS NO:632332-46-8
Molecular Formula:
Molecular Weight: 514.737
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: Acrylic acid (1S,2R)-1-benzyloxymethyl-2-(tert-butyl-diphenyl-silanyloxymethyl)-but-3-enyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acrylic acid (1S,2R)-1-benzyloxymethyl-2-(tert-butyl-diphenyl-silanyloxymethyl)-but-3-enyl ester(632332-46-8)
EPA Substance Registry System: Acrylic acid (1S,2R)-1-benzyloxymethyl-2-(tert-butyl-diphenyl-silanyloxymethyl)-but-3-enyl ester(632332-46-8)

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: 632332-46-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 632332-46-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,2,3,3 and 2 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 632332-46:
(8*6)+(7*3)+(6*2)+(5*3)+(4*3)+(3*2)+(2*4)+(1*6)=128
128 % 10 = 8
So 632332-46-8 is a valid CAS Registry Number.

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632332-46-8Relevant academic research and scientific papers

Enantioselective synthesis of mono- and disubstituted 3, 6-dihydro-2H-pyrans and 5,6-dihydropyran-2-ones

Izzo, Irene,Del Gaudio, Pasquale,Della Monica, Carmela,Squitieri, Maria,De Riccardis, Francesco

, p. 2057 - 2063 (2007/10/03)

An enantioselective synthesis of mono- and disubstituted 3,6-dihydro-2H-pyrans and 5,6-dihydropyran-2-ones was achieved via ring-closing olefin metathesis, employing Grubb's catalyst, and starting from ready available chiral building blocks.

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