Cas 872216-01-8,(2S,5S,6S)-6-tert-butyldimethylsilyloxy-2,5-dihydroxyoctadecanyl 2',4',6'-triisopropylbenzenesulfonate

872216-01-8

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Basic information

Product Name: (2S,5S,6S)-6-tert-butyldimethylsilyloxy-2,5-dihydroxyoctadecanyl 2',4',6'-triisopropylbenzenesulfonate
Synonyms: (2S,5S,6S)-6-tert-butyldimethylsilyloxy-2,5-dihydroxyoctadecanyl 2',4',6'-triisopropylbenzenesulfonate
CAS NO:872216-01-8
Molecular Formula:
Molecular Weight: 699.164
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,5S,6S)-6-tert-butyldimethylsilyloxy-2,5-dihydroxyoctadecanyl 2',4',6'-triisopropylbenzenesulfonate(CAS DataBase Reference)
NIST Chemistry Reference: (2S,5S,6S)-6-tert-butyldimethylsilyloxy-2,5-dihydroxyoctadecanyl 2',4',6'-triisopropylbenzenesulfonate(872216-01-8)
EPA Substance Registry System: (2S,5S,6S)-6-tert-butyldimethylsilyloxy-2,5-dihydroxyoctadecanyl 2',4',6'-triisopropylbenzenesulfonate(872216-01-8)

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: 872216-01-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 872216-01-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,2,2,1 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 872216-01:
(8*8)+(7*7)+(6*2)+(5*2)+(4*1)+(3*6)+(2*0)+(1*1)=158
158 % 10 = 8
So 872216-01-8 is a valid CAS Registry Number.

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872216-01-8Relevant academic research and scientific papers

Total synthesis of murisolins and evaluation of tumor-growth inhibitory activity

Maezaki, Naoyoshi,Tominaga, Hiroaki,Kojima, Naoto,Yanai, Minori,Urabe, Daisuke,Ueki, Risa,Tanaka, Tetsuaki,Yamori, Takao

, p. 6237 - 6245 (2007/10/03)

Convergent total syntheses of murisolin (1), natural 16,19-cis-murisolin 2, and unnatural 16,19-cis-murisolin 3 were accomplished by asymmetric alkynylation of α-tetrahydrofuranic aldehyde with a diyne and Sonogashira coupling with a γ-lactone segment as

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