Cas 1092695-82-3,{[(E,4Z)-6-(benzyloxy)-4-chlorohexa-2,4-dien-1-yl]oxy}(tert-butyl)diphenylsilane

1092695-82-3

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Basic information

Product Name: {[(E,4Z)-6-(benzyloxy)-4-chlorohexa-2,4-dien-1-yl]oxy}(tert-butyl)diphenylsilane
Synonyms: {[(E,4Z)-6-(benzyloxy)-4-chlorohexa-2,4-dien-1-yl]oxy}(tert-butyl)diphenylsilane
CAS NO:1092695-82-3
Molecular Formula:
Molecular Weight: 477.118
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: {[(E,4Z)-6-(benzyloxy)-4-chlorohexa-2,4-dien-1-yl]oxy}(tert-butyl)diphenylsilane(CAS DataBase Reference)
NIST Chemistry Reference: {[(E,4Z)-6-(benzyloxy)-4-chlorohexa-2,4-dien-1-yl]oxy}(tert-butyl)diphenylsilane(1092695-82-3)
EPA Substance Registry System: {[(E,4Z)-6-(benzyloxy)-4-chlorohexa-2,4-dien-1-yl]oxy}(tert-butyl)diphenylsilane(1092695-82-3)

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: 1092695-82-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1092695-82-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,2,6,9 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1092695-82:
(9*1)+(8*0)+(7*9)+(6*2)+(5*6)+(4*9)+(3*5)+(2*8)+(1*2)=183
183 % 10 = 3
So 1092695-82-3 is a valid CAS Registry Number.

1092695-82-3Upstream product

1092696-00-8 C₂₉H₃₄O₃Si

1092695-82-3Downstream Products

1092695-82-3Relevant academic research and scientific papers

Enantiocontrolled synthesis of polychlorinated hydrocarbon motifs: A nucleophilic multiple chlorination process revisited

Yoshimitsu, Takehiko,Fukumoto, Naoya,Tanaka, Tetsuaki

, p. 696 - 702 (2009)

Polychlorinated hydrocarbon motifs have been synthesized in enantiomerically pure forms by means of nucleophilic multiple chlorinations of chiral epoxides, which stereospecifically incorporate halogen atoms into oxygenated molecular scaffolds. The present

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