Cas 185693-88-3,Silane, trimethyl[2-[(4-methylphenyl)sulfonyl]-2-phenyl-1-[(phenylmethoxy)methyl] ethoxy]-

185693-88-3

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Basic information

Product Name: Silane, trimethyl[2-[(4-methylphenyl)sulfonyl]-2-phenyl-1-[(phenylmethoxy)methyl] ethoxy]-
Synonyms:
CAS NO:185693-88-3
Molecular Formula: C26H32O4SSi
Molecular Weight:
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: Silane, trimethyl[2-[(4-methylphenyl)sulfonyl]-2-phenyl-1-[(phenylmethoxy)methyl] ethoxy]-(CAS DataBase Reference)
NIST Chemistry Reference: Silane, trimethyl[2-[(4-methylphenyl)sulfonyl]-2-phenyl-1-[(phenylmethoxy)methyl] ethoxy]-(185693-88-3)
EPA Substance Registry System: Silane, trimethyl[2-[(4-methylphenyl)sulfonyl]-2-phenyl-1-[(phenylmethoxy)methyl] ethoxy]-(185693-88-3)

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: 185693-88-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 185693-88-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,5,6,9 and 3 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 185693-88:
(8*1)+(7*8)+(6*5)+(5*6)+(4*9)+(3*3)+(2*8)+(1*8)=193
193 % 10 = 3
So 185693-88-3 is a valid CAS Registry Number.

185693-88-3Upstream product

185693-88-3Downstream Products

954-55-2 2,3-diphenylfuran

185693-88-3Relevant academic research and scientific papers

(Alkoxyallyl)sulfones as enal and enone β-anion equivalents. Synthesis of mono-, di- and trisubstituted furans

Craig, Donald,Etheridge, Christopher J.

, p. 15289 - 15310 (2007/10/03)

Treatment of variously-substituted (alkoxyallyl)sulfones 1, 7-9 with strong base followed by aldehydes gives alcohol adducts 5. These may be converted into a wide range of substituted furans 6 by exposure to acid, or to silica gel in dichloromethane containing sulfuric acid in some cases.

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