Cas 252062-23-0,3-cyclohexyl-3-(dimethylphenylsilyl)-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-propene

252062-23-0

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Basic information

Product Name: 3-cyclohexyl-3-(dimethylphenylsilyl)-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-propene
Synonyms: 3-cyclohexyl-3-(dimethylphenylsilyl)-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-propene
CAS NO:252062-23-0
Molecular Formula:
Molecular Weight: 384.442
EINECS: N/A
Product Categories: N/A
Mol File: 252062-23-0.mol
Article Data: 2

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: 3-cyclohexyl-3-(dimethylphenylsilyl)-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-propene(CAS DataBase Reference)
NIST Chemistry Reference: 3-cyclohexyl-3-(dimethylphenylsilyl)-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-propene(252062-23-0)
EPA Substance Registry System: 3-cyclohexyl-3-(dimethylphenylsilyl)-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-propene(252062-23-0)

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: 252062-23-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 252062-23-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,2,0,6 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 252062-23:
(8*2)+(7*5)+(6*2)+(5*0)+(4*6)+(3*2)+(2*2)+(1*3)=100
100 % 10 = 0
So 252062-23-0 is a valid CAS Registry Number.

252062-23-0Upstream product

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252062-23-0Relevant articles and documents

Highly regioselective silaboration of 3-substituted 1,2-dienes catalyzed by palladium/2,6-xylyl isocyanide

Suginome, Michinori,Ohmori, Yutaka,Ito, Yoshihiko

, p. 1567 - 1568 (1999)

Regioselective silaboration of 3-substituted 1,2-dienes was efficiently catalyzed by palladium/2,6-xylyl isocyanide complex, affording an adduct, in which the boryl and silyl groups were introduced at the central allenyl carbon and at the substituted alle

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