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18737-73-0

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18737-73-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18737-73-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,7,3 and 7 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 18737-73:
(7*1)+(6*8)+(5*7)+(4*3)+(3*7)+(2*7)+(1*3)=140
140 % 10 = 0
So 18737-73-0 is a valid CAS Registry Number.

18737-73-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name triphenyl(propyl)silane

1.2 Other means of identification

Product number -
Other names triphenylsilylpropane

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:18737-73-0 SDS

18737-73-0Downstream Products

18737-73-0Relevant articles and documents

Catalytic protodeboronation of pinacol boronic esters: Formal anti-Markovnikov hydromethylation of alkenes

Clausen, Florian,Kischkewitz, Marvin,Bergander, Klaus,Studer, Armido

, p. 6210 - 6214 (2019/06/27)

Pinacol boronic esters are highly valuable building blocks in organic synthesis. In contrast to the many protocols available on the functionalizing deboronation of alkyl boronic esters, protodeboronation is not well developed. Herein we report catalytic protodeboronation of 1°, 2° and 3° alkyl boronic esters utilizing a radical approach. Paired with a Matteson-CH2-homologation, our protocol allows for formal anti-Markovnikov alkene hydromethylation, a valuable but unknown transformation. The hydromethylation sequence was applied to methoxy protected (-)-Δ8-THC and cholesterol. The protodeboronation was further used in the formal total synthesis of δ-(R)-coniceine and indolizidine 209B.

Tandem reaction by using compatible catalysts: Cross-metathesis reaction and hydrogenation

Cossy, Janine,Bargiggia, Frédéric C.,BouzBouz, Samir

, p. 6715 - 6717 (2007/10/03)

A one-pot tandem cross-metathesis/hydrogenation procedure was achieved at room temperature, under one atmosphere of hydrogen, in the presence of ruthenium catalyst II and PtO2 showing the compatibility of the two catalysts.

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