Cas 924364-21-6,(S,E)-6-(tert-butyldiphenylsilyloxy)-2-(cyclohexylmethyl)hex-4-en-1-ol

924364-21-6

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Basic information

Product Name: (S,E)-6-(tert-butyldiphenylsilyloxy)-2-(cyclohexylmethyl)hex-4-en-1-ol
Synonyms: (S,E)-6-(tert-butyldiphenylsilyloxy)-2-(cyclohexylmethyl)hex-4-en-1-ol
CAS NO:924364-21-6
Molecular Formula:
Molecular Weight: 450.737
EINECS: N/A
Product Categories: N/A
Mol File: 924364-21-6.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,E)-6-(tert-butyldiphenylsilyloxy)-2-(cyclohexylmethyl)hex-4-en-1-ol(CAS DataBase Reference)
NIST Chemistry Reference: (S,E)-6-(tert-butyldiphenylsilyloxy)-2-(cyclohexylmethyl)hex-4-en-1-ol(924364-21-6)
EPA Substance Registry System: (S,E)-6-(tert-butyldiphenylsilyloxy)-2-(cyclohexylmethyl)hex-4-en-1-ol(924364-21-6)

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: 924364-21-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 924364-21-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,4,3,6 and 4 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 924364-21:
(8*9)+(7*2)+(6*4)+(5*3)+(4*6)+(3*4)+(2*2)+(1*1)=166
166 % 10 = 6
So 924364-21-6 is a valid CAS Registry Number.

924364-21-6Upstream product

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924364-21-6Relevant articles and documents

Asymmetric synthesis of α-substituted aldehydes by Pd-catalyzed asymmetric allylic alkylation-alkene isomerization-Claisen rearrangement

Trost, Barry M.,Zhang, Ting

, p. 6007 - 6010 (2007/10/03)

(Chemical Equation Presented) Enantiospecific aliphatic Claisen rearrangement was realized with generally high chirality transfer. The requisite substrates were synthesized via Pd-catalyzed asymmetric allylic alkylation (AAA) from easily obtained starting

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