Cas 321995-82-8,(2S,3S,4S,5S,6R)-1,7-dibenzyloxy-2,4,6-trimethyl-3,5-[[bis(1,1-dimethylethyl)-silylene]dioxy]-heptane

321995-82-8

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Basic information

Product Name: (2S,3S,4S,5S,6R)-1,7-dibenzyloxy-2,4,6-trimethyl-3,5-[[bis(1,1-dimethylethyl)-silylene]dioxy]-heptane
Synonyms: (2S,3S,4S,5S,6R)-1,7-dibenzyloxy-2,4,6-trimethyl-3,5-[[bis(1,1-dimethylethyl)-silylene]dioxy]-heptane
CAS NO:321995-82-8
Molecular Formula:
Molecular Weight: 526.832
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,3S,4S,5S,6R)-1,7-dibenzyloxy-2,4,6-trimethyl-3,5-[[bis(1,1-dimethylethyl)-silylene]dioxy]-heptane(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3S,4S,5S,6R)-1,7-dibenzyloxy-2,4,6-trimethyl-3,5-[[bis(1,1-dimethylethyl)-silylene]dioxy]-heptane(321995-82-8)
EPA Substance Registry System: (2S,3S,4S,5S,6R)-1,7-dibenzyloxy-2,4,6-trimethyl-3,5-[[bis(1,1-dimethylethyl)-silylene]dioxy]-heptane(321995-82-8)

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: 321995-82-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 321995-82-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,1,9,9 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 321995-82:
(8*3)+(7*2)+(6*1)+(5*9)+(4*9)+(3*5)+(2*8)+(1*2)=158
158 % 10 = 8
So 321995-82-8 is a valid CAS Registry Number.

321995-82-8Upstream product

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321995-82-8Relevant academic research and scientific papers

Stereoselective synthesis of dihydropyrone-containing marine natural products. Total synthesis and structural elucidation of (-)-membrenone-C.

Perkins,Sampson

, p. 123 - 126 (2007/10/03)

[figure: see text] Three diastereomers of membrenone-C were separately prepared using a common two directional chain extending synthetic strategy. This has established the absolute and relative configuration of the natural product to be as shown in the fo

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