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18246-06-5

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18246-06-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18246-06-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,2,4 and 6 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 18246-06:
(7*1)+(6*8)+(5*2)+(4*4)+(3*6)+(2*0)+(1*6)=105
105 % 10 = 5
So 18246-06-5 is a valid CAS Registry Number.

18246-06-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name chloro(dimethoxy)phenylsilane

1.2 Other means of identification

Product number -
Other names Chlor-dimethoxy-phenyl-silan

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:18246-06-5 SDS

18246-06-5Relevant articles and documents

Direct alkoxysilylation of alkoxysilanes for the synthesis of explicit alkoxysiloxane oligomers

Wakabayashi, Ryutaro,Tamai, Misa,Kawahara, Kazufumi,Tachibana, Hiroki,Imamura, Yutaka,Nakai, Hiromi,Kuroda, Kazuyuki

, p. 26 - 31 (2012/11/13)

Direct alkoxysilylation, which is a powerful tool to provide explicit alkoxysiloxanes, is developed and its versatility is investigated. Siloxane pentamers Si[OSiR1(OMe)2]4 having various functional groups (R1 = methyl, vinyl, phenyl, chloropropyl and n-butyl groups) were successfully obtained by direct alkoxysilylation of Si(OR)4 (R = t-Bu, CHPh2). Thus, the versatility of the reaction is confirmed on organic functional groups R1. Functional group tolerance of the reaction is discussed on the basis of electronegativity of the R1 groups. Alkoxysilylation of Si(Ot-Bu)2(OMe) 2 and Si(Ot-Bu)(OMe)3 selectively gives trimer (MeO) 2Si[OSiMe(OMe)2]2 and dimer (MeO) 3SiOSiMe(OMe)2, respectively. Thus, the feasibility on siloxane structure is also confirmed. Various siloxane compounds are synthesized by this newly developed reaction for the first time.

Reaction of Tetraalkoxysilanes with Alkyl(aryl)chlorosilanes

Chernyshev, E. A.,Komalenkova, N. G.,Tagachenkov, A. A.,Bykovchenko, V. G.

, p. 241 - 243 (2007/10/03)

Alkyl(aryl)trichloro- or dialkyl(diaryl)dichlorosilanes react with tetraalkoxysilanes Si(OMe)4, Si(OEt)4, and Si(OBu)4 to give partially etherfied alkyl(aryl)chlorosilanes RSiCl2(OAlk), RSiCl(OAlk)2, and R2SiCl(OAlk).

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