Cas 1628173-08-9,dimethyl(1-(naphthalen-1-yl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)propan-2-yl)(phenyl)silane

1628173-08-9

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Basic information

Product Name: dimethyl(1-(naphthalen-1-yl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)propan-2-yl)(phenyl)silane
Synonyms: dimethyl(1-(naphthalen-1-yl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)propan-2-yl)(phenyl)silane
CAS NO:1628173-08-9
Molecular Formula:
Molecular Weight: 430.47
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: dimethyl(1-(naphthalen-1-yl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)propan-2-yl)(phenyl)silane(CAS DataBase Reference)
NIST Chemistry Reference: dimethyl(1-(naphthalen-1-yl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)propan-2-yl)(phenyl)silane(1628173-08-9)
EPA Substance Registry System: dimethyl(1-(naphthalen-1-yl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)propan-2-yl)(phenyl)silane(1628173-08-9)

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: 1628173-08-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1628173-08-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,2,8,1,7 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1628173-08:
(9*1)+(8*6)+(7*2)+(6*8)+(5*1)+(4*7)+(3*3)+(2*0)+(1*8)=169
169 % 10 = 9
So 1628173-08-9 is a valid CAS Registry Number.

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1628173-08-9Relevant academic research and scientific papers

Three-component carboboration of alkenes under copper catalysis

Kageyuki, Ikuo,Yoshida, Hiroto,Takaki, Ken

, p. 1924 - 1932 (2014)

Three-component carboboration of alkenes takes place efficiently by the reaction with a diboron compound and carbon electrophiles with the aid of a copper-NHC catalyst. The carboboration afforded diverse multisubstituted borylalkanes via the regioselective formation of carbon-boron and carbon-carbon bonds. Georg Thieme Verlag Stuttgart New Yorks.

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