Cas 114964-60-2,(R)-3-{2-[(S)-(Methyl-diphenyl-silanyloxy)-phenyl-methyl]-[1,3]dithian-2-yl}-butan-1-ol

114964-60-2

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Basic information

Product Name: (R)-3-{2-[(S)-(Methyl-diphenyl-silanyloxy)-phenyl-methyl]-[1,3]dithian-2-yl}-butan-1-ol
Synonyms:
CAS NO:114964-60-2
Molecular Formula:
Molecular Weight: 494.794
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: (R)-3-{2-[(S)-(Methyl-diphenyl-silanyloxy)-phenyl-methyl]-[1,3]dithian-2-yl}-butan-1-ol(CAS DataBase Reference)
NIST Chemistry Reference: (R)-3-{2-[(S)-(Methyl-diphenyl-silanyloxy)-phenyl-methyl]-[1,3]dithian-2-yl}-butan-1-ol(114964-60-2)
EPA Substance Registry System: (R)-3-{2-[(S)-(Methyl-diphenyl-silanyloxy)-phenyl-methyl]-[1,3]dithian-2-yl}-butan-1-ol(114964-60-2)

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: 114964-60-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 114964-60-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,9,6 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 114964-60:
(8*1)+(7*1)+(6*4)+(5*9)+(4*6)+(3*4)+(2*6)+(1*0)=132
132 % 10 = 2
So 114964-60-2 is a valid CAS Registry Number.

114964-60-2Upstream product

144-79-6 chloromethyldiphenylsilane

114964-60-2Downstream Products

114964-60-2Relevant academic research and scientific papers

1,3-Asymmetric Induction in Acyclic Systems by Practical Application of Dithioacetal Group

Honda, Yutaka,Morita, Eitaro,Ohshiro, Kimitaka,Tsuchihashi, Gen-ichi

, p. 21 - 24 (1988)

2-Lithio-2-(1-methyl-2-alkenyl)-1,3-dithianes showed 1,3-syn-selectivity on addition to aldehydes.Moreover this selectivity could be increased up to 97percent de by using equilibration of potassium alkoxide of the adduct in the presence of a ligand.

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