Cas 201991-65-3,[(Z)-(3R,4S,5S)-2,3,4,5-Tetrakis-(tert-butyl-dimethyl-silanyloxy)-6,6-dimethoxy-hex-1-ene-1-sulfonyl]-benzene

201991-65-3

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Basic information

Product Name: [(Z)-(3R,4S,5S)-2,3,4,5-Tetrakis-(tert-butyl-dimethyl-silanyloxy)-6,6-dimethoxy-hex-1-ene-1-sulfonyl]-benzene
Synonyms: [(Z)-(3R,4S,5S)-2,3,4,5-Tetrakis-(tert-butyl-dimethyl-silanyloxy)-6,6-dimethoxy-hex-1-ene-1-sulfonyl]-benzene
CAS NO:201991-65-3
Molecular Formula:
Molecular Weight: 805.425
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: [(Z)-(3R,4S,5S)-2,3,4,5-Tetrakis-(tert-butyl-dimethyl-silanyloxy)-6,6-dimethoxy-hex-1-ene-1-sulfonyl]-benzene(CAS DataBase Reference)
NIST Chemistry Reference: [(Z)-(3R,4S,5S)-2,3,4,5-Tetrakis-(tert-butyl-dimethyl-silanyloxy)-6,6-dimethoxy-hex-1-ene-1-sulfonyl]-benzene(201991-65-3)
EPA Substance Registry System: [(Z)-(3R,4S,5S)-2,3,4,5-Tetrakis-(tert-butyl-dimethyl-silanyloxy)-6,6-dimethoxy-hex-1-ene-1-sulfonyl]-benzene(201991-65-3)

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: 201991-65-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 201991-65-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,1,9,9 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 201991-65:
(8*2)+(7*0)+(6*1)+(5*9)+(4*9)+(3*1)+(2*6)+(1*5)=123
123 % 10 = 3
So 201991-65-3 is a valid CAS Registry Number.

201991-65-3Upstream product

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201991-65-3Relevant academic research and scientific papers

Total synthesis of a glyoxalase I inhibitor and its precursor, (-)-KD16-U1

Tatsuta, Kuniaki,Yasuda, Shohei,Araki, Nobuyuki,Takahashi, Masaaki,Kamiya, Yuko

, p. 401 - 402 (2007/10/03)

A glyoxalase I inhibitor and (-)-KD16-U1 have been synthesized from D-ribonic acid γ-lactone through SnCl4-promoted cyclization of a phenylsulfonyl enol silyl ether and regioselective introduction of a hydroxymethyl group.

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