Cas 803699-27-6,(S)-1-{(4R,5S,6R)-6-[(S)-2-(tert-Butyl-diphenyl-silanyloxy)-1-methyl-ethyl]-2,2,5-trimethyl-[1,3]dioxan-4-yl}-ethanol

803699-27-6

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Basic information

Product Name: (S)-1-{(4R,5S,6R)-6-[(S)-2-(tert-Butyl-diphenyl-silanyloxy)-1-methyl-ethyl]-2,2,5-trimethyl-[1,3]dioxan-4-yl}-ethanol
Synonyms: (S)-1-{(4R,5S,6R)-6-[(S)-2-(tert-Butyl-diphenyl-silanyloxy)-1-methyl-ethyl]-2,2,5-trimethyl-[1,3]dioxan-4-yl}-ethanol
CAS NO:803699-27-6
Molecular Formula:
Molecular Weight: 470.725
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)-1-{(4R,5S,6R)-6-[(S)-2-(tert-Butyl-diphenyl-silanyloxy)-1-methyl-ethyl]-2,2,5-trimethyl-[1,3]dioxan-4-yl}-ethanol(CAS DataBase Reference)
NIST Chemistry Reference: (S)-1-{(4R,5S,6R)-6-[(S)-2-(tert-Butyl-diphenyl-silanyloxy)-1-methyl-ethyl]-2,2,5-trimethyl-[1,3]dioxan-4-yl}-ethanol(803699-27-6)
EPA Substance Registry System: (S)-1-{(4R,5S,6R)-6-[(S)-2-(tert-Butyl-diphenyl-silanyloxy)-1-methyl-ethyl]-2,2,5-trimethyl-[1,3]dioxan-4-yl}-ethanol(803699-27-6)

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: 803699-27-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 803699-27-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,0,3,6,9 and 9 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 803699-27:
(8*8)+(7*0)+(6*3)+(5*6)+(4*9)+(3*9)+(2*2)+(1*7)=186
186 % 10 = 6
So 803699-27-6 is a valid CAS Registry Number.

803699-27-6Upstream product

803699-27-6Downstream Products

82294-14-2 (2R,3S,4S,5R)-1-tert-butyldiphenylsilyloxy-2,4-dimethyl-3,5-isopropylidenedioxyheptan-6-one

803699-27-6Relevant academic research and scientific papers

Double stereodifferentiating aldol reactions based on chiral ketones derived from lactic acid: Synthesis of C1-C6 fragment of erythronolides

Solsona, Joan G.,Nebot, Joaquim,Romea, Pedro,Urpí, Fèlix

, p. 2127 - 2130 (2007/10/03)

Highly stereoselective titanium-mediated aldol additions of ethyl ketones derived from lactic acid to α-methyl-β-OTBDPS chiral aldehydes are documented. One of these double stereodifferentiating processes represents the key step of a straightforward and e

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