Cas 120341-99-3,(S)-6-(tert-Butyl-diphenyl-silanyloxy)-1-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-hexan-2-ol

120341-99-3

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Basic information

Product Name: (S)-6-(tert-Butyl-diphenyl-silanyloxy)-1-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-hexan-2-ol
Synonyms:
CAS NO:120341-99-3
Molecular Formula:
Molecular Weight: 456.698
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: (S)-6-(tert-Butyl-diphenyl-silanyloxy)-1-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-hexan-2-ol(CAS DataBase Reference)
NIST Chemistry Reference: (S)-6-(tert-Butyl-diphenyl-silanyloxy)-1-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-hexan-2-ol(120341-99-3)
EPA Substance Registry System: (S)-6-(tert-Butyl-diphenyl-silanyloxy)-1-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-hexan-2-ol(120341-99-3)

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: 120341-99-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 120341-99-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,3,4 and 1 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 120341-99:
(8*1)+(7*2)+(6*0)+(5*3)+(4*4)+(3*1)+(2*9)+(1*9)=83
83 % 10 = 3
So 120341-99-3 is a valid CAS Registry Number.

120341-99-3Upstream product

120341-95-9 6-(tert-Butyl-diphenyl-silanyloxy)-1-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-hexan-2-one

120341-99-3Downstream Products

120341-99-3Relevant academic research and scientific papers

STEREOSELECTIVE REDUCTION OF β-ALKOXY KETONES: A SYNTHESIS OF SYN-1,3-DIOLS

Mori, Yuji,Kuhara, Miki,Takeuchi, Akio,Suzuki, Makoto

, p. 5419 - 5422 (1988)

The diastereoselective reduction of acyclic β-alkoxy ketones with lithium aluminum hydride in the presence of lithium iodide has been studied and found to provide syn-1,3-diol derivatives with high diastereoselection.

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