Cas 199010-68-9,8-[2-Benzenesulfonyl-1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazol-4-yl]-1,4-dioxa-spiro[4.5]decan-8-ol

199010-68-9

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Basic information

Product Name: 8-[2-Benzenesulfonyl-1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazol-4-yl]-1,4-dioxa-spiro[4.5]decan-8-ol
Synonyms: 8-[2-Benzenesulfonyl-1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazol-4-yl]-1,4-dioxa-spiro[4.5]decan-8-ol
CAS NO:199010-68-9
Molecular Formula:
Molecular Weight: 494.684
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: 8-[2-Benzenesulfonyl-1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazol-4-yl]-1,4-dioxa-spiro[4.5]decan-8-ol(CAS DataBase Reference)
NIST Chemistry Reference: 8-[2-Benzenesulfonyl-1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazol-4-yl]-1,4-dioxa-spiro[4.5]decan-8-ol(199010-68-9)
EPA Substance Registry System: 8-[2-Benzenesulfonyl-1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazol-4-yl]-1,4-dioxa-spiro[4.5]decan-8-ol(199010-68-9)

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: 199010-68-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 199010-68-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,9,0,1 and 0 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 199010-68:
(8*1)+(7*9)+(6*9)+(5*0)+(4*1)+(3*0)+(2*6)+(1*8)=149
149 % 10 = 9
So 199010-68-9 is a valid CAS Registry Number.

199010-68-9Upstream product

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199010-68-9Relevant academic research and scientific papers

1-[2'-(trimethylsilyl)ethoxymethyl]-2-phenylsulfonylimidazole: A new reagent for the preparation of C-4 substituted imidazoles

Phillips, James G.,Fadnis, Leena,Williams, David R.

, p. 7835 - 7838 (2007/10/03)

The title compound provides for the efficient C-4 metallation of the imidazole nucleus. Further reactions lead to trisubstituted imidazoles which can be selectively deprotected at the N1 and C2 positions under mild conditions to maximize the potential for further elaboration.

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