Cas 187334-63-0,[(2S,4R,6R)-6-(tert-Butyl-dimethyl-silanyloxy)-4-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-pyran-2-yl]-acetaldehyde

187334-63-0

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Basic information

Product Name: [(2S,4R,6R)-6-(tert-Butyl-dimethyl-silanyloxy)-4-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-pyran-2-yl]-acetaldehyde
Synonyms:
CAS NO:187334-63-0
Molecular Formula:
Molecular Weight: 512.837
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,4R,6R)-6-(tert-Butyl-dimethyl-silanyloxy)-4-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-pyran-2-yl]-acetaldehyde(CAS DataBase Reference)
NIST Chemistry Reference: [(2S,4R,6R)-6-(tert-Butyl-dimethyl-silanyloxy)-4-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-pyran-2-yl]-acetaldehyde(187334-63-0)
EPA Substance Registry System: [(2S,4R,6R)-6-(tert-Butyl-dimethyl-silanyloxy)-4-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-pyran-2-yl]-acetaldehyde(187334-63-0)

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: 187334-63-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 187334-63-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,7,3,3 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 187334-63:
(8*1)+(7*8)+(6*7)+(5*3)+(4*3)+(3*4)+(2*6)+(1*3)=160
160 % 10 = 0
So 187334-63-0 is a valid CAS Registry Number.

187334-63-0Upstream product

187334-63-0Downstream Products

187334-64-1 2-[(2R,4R,6R)-6-(tert-Butyl-dimethyl-silanyloxy)-4-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-pyran-2-yl]-ethanol

187334-63-0Relevant academic research and scientific papers

Asymmetric synthesis of the δ-lactone moiety in mevinic acid derivatives using an enzymatic procedure

Kaku, Hidetaka,Tanaka, Masakazu,Norimine, Yoshihiko,Miyashita, Yuko,Suemune, Hiroshi,Sakai, Kiyoshi

, p. 195 - 201 (2007/10/03)

Asymmetric induction into meso-1,3-diacetoxy-5-cycloheptene 4 by PFL-catalyzed hydrolysis afforded monoacetate (1S,3R)-5 of 96% enantiomeric excess (e.e.), which was converted into a synthetic equivalent 14 of the δ-lactone moiety in mevinic acid derivatives.

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