Cas 217964-65-3,[(2R,5R,6S)-7-(tert-Butyl-dimethyl-silanyloxy)-2,6-dimethyl-3-methylene-5-trimethylsilanyloxy-heptyloxymethyl]-benzene

217964-65-3

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Basic information

Product Name: [(2R,5R,6S)-7-(tert-Butyl-dimethyl-silanyloxy)-2,6-dimethyl-3-methylene-5-trimethylsilanyloxy-heptyloxymethyl]-benzene
Synonyms: [(2R,5R,6S)-7-(tert-Butyl-dimethyl-silanyloxy)-2,6-dimethyl-3-methylene-5-trimethylsilanyloxy-heptyloxymethyl]-benzene
CAS NO:217964-65-3
Molecular Formula:
Molecular Weight: 464.836
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: [(2R,5R,6S)-7-(tert-Butyl-dimethyl-silanyloxy)-2,6-dimethyl-3-methylene-5-trimethylsilanyloxy-heptyloxymethyl]-benzene(CAS DataBase Reference)
NIST Chemistry Reference: [(2R,5R,6S)-7-(tert-Butyl-dimethyl-silanyloxy)-2,6-dimethyl-3-methylene-5-trimethylsilanyloxy-heptyloxymethyl]-benzene(217964-65-3)
EPA Substance Registry System: [(2R,5R,6S)-7-(tert-Butyl-dimethyl-silanyloxy)-2,6-dimethyl-3-methylene-5-trimethylsilanyloxy-heptyloxymethyl]-benzene(217964-65-3)

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: 217964-65-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 217964-65-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,7,9,6 and 4 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 217964-65:
(8*2)+(7*1)+(6*7)+(5*9)+(4*6)+(3*4)+(2*6)+(1*5)=163
163 % 10 = 3
So 217964-65-3 is a valid CAS Registry Number.

217964-65-3Upstream product

217964-65-3Downstream Products

217964-65-3Relevant academic research and scientific papers

On 1,4-diastereoselectivity in the chiral allylsilane addition to chiral α-substituted aldehydes

Dias, Luiz C.,Giacomini, Rosana

, p. 5343 - 5346 (2007/10/03)

Chiral allyisilane 2 reacted with chiral α-substituted aldehydes to afford the corresponding 1,4-syn-products with good diastereoseletivities. The best selectivities are observe when the reactions are carried out by transmetallation of allylsilane using T

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