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36147-65-6

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36147-65-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36147-65-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,1,4 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 36147-65:
(7*3)+(6*6)+(5*1)+(4*4)+(3*7)+(2*6)+(1*5)=116
116 % 10 = 6
So 36147-65-6 is a valid CAS Registry Number.

36147-65-6SDS

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 trichloro-[[2-(chloromethyl)phenyl]methyl]silane

1.2 Other means of identification

Product number -
Other names Silane,trichloro[[2-(chloromethyl)phenyl]methyl]

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:36147-65-6 SDS

36147-65-6Downstream Products

36147-65-6Relevant articles and documents

Dehydrohalogenative coupling reaction of organic halides with silanes

-

, (2008/06/13)

The present invention relates to methods for making the compounds of formula I which is a dehydrohalogenative coupling of hydrochlorosilanes of formula II with organic halides of formula III in the presence of a Lewis base catalyst. R3CH2SiR1Cl2??(I) HSiR1Cl2??(II) R2CH2X??(III) In formulas I and II, R1represents a hydrogen, chloro, or methyl; in formula III, X represents a chloro or bromo; in formula III, R2can be selected from the group consisting of a C1-17alkyl, a C1-10fluorinated alkyl with partial or full fluorination, a C1-5alkenyl groups, a silyl group containing alkyls, (CH2)nSiMe3-mClmwherein n is 0 to 2 and m is 0 to 3, aromatic groups, Ar(R′)1wherein Ar is C6-14aromatic hydrocarbon, R′ is a C1-4alkyl, halogen, alkoxy, or vinyl, and q is 0 to 5, a haloalkyl group, (CH2)pX wherein p is 1 to 9 and X is a chloro or bromo; or an aromatic hydrocarbon, Ar CH2X wherein Ar is C6-14aromatic hydrocarbon and X is a chloro or bromo. in formula I, R3is the same as R2in formula III and further, R3can also be (CH2)pSiR1Cl2or ArCH2SiR1Cl2when R2in formula III is (CH2)pX or ArCH2X, because of the coupling reaction of X with the compound of formula II.

ONE-STEP REGIOSPECIFIC SYNTHESIS OF ALLYLIC SILANES - EXTENSION TO BENZYLSILANES

Lefort, Marcel,Simmonet, Christian,Birot, Marc,Deleris, Gerard,Dunogues, Jacques,Calas, Raymond

, p. 1857 - 1860 (2007/10/02)

Allyltrichlorosilanes are prepared according to a one-step regiospecific process based on the reaction of allyl chlorides with SiCl4 and NiCp2/HMPA (catalyst), in the presence of industrial methylchlorodisilane fraction.Benzyltrihalosilanes are similarly obtained.

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