Welcome to LookChem.com Sign In|Join Free

CAS

  • or

812-36-2

Post Buying Request

812-36-2 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

812-36-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 812-36-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,1 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 812-36:
(5*8)+(4*1)+(3*2)+(2*3)+(1*6)=62
62 % 10 = 2
So 812-36-2 is a valid CAS Registry Number.

812-36-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name bis[chloro(dimethyl)silyl]-dimethylsilane

1.2 Other means of identification

Product number -
Other names ClMe2SiSiMe2Cl

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:812-36-2 SDS

812-36-2Relevant articles and documents

DISILANE-, CARBODISILANE-AND OLIGOSILANE CLEAVAGE WITH CLEAVAGE COMPOUND ACTING AS CATALYST AND HYDROGENATION SOURCE

-

Page/Page column 44, (2019/04/16)

The invention relates to a process for the manufacture of monosilanes of formula (I): MexSiHyClz (I), comprising: the step of subjecting a silane substrate (methyldisilanes, methyloligosilanes, or carbodisilanes) to a cleavage reaction of the silicon-silicon bond(s) or the silicon- carbon bonds in silane substrates the reaction involving a cleavage compound selected from a quaternary Group 15 onium compound R4 QX, a heterocyclic amine, a heterocyclic ammonium halide, or a mixture of R3P and RX. The starting material disilanes to be cleaved has the formula (II): MemSi2HnClo (II) The starting material oligosilanes to be cleaved have the general formula (III): MepSiqHrCIs (II I), The starting material carbodisilanes to be cleaved have the general formula (IV): (MeaSiHbCle)-CH2-(MecSiHdClf) (IV)

Conductive molecular silicon

Klausen, Rebekka S.,Widawsky, Jonathan R.,Steigerwald, Michael L.,Venkataraman, Latha,Nuckolls, Colin

supporting information; experimental part, p. 4541 - 4544 (2012/04/23)

Bulk silicon, the bedrock of information technology, consists of the deceptively simple electronic structure of just Si-Si σ bonds. Diamond has the same lattice structure as silicon, yet the two materials have dramatically different electronic properties. Here we report the specific synthesis and electrical characterization of a class of molecules, oligosilanes, that contain strongly interacting Si-Si σ bonds, the essential components of the bulk semiconductor. We used the scanning tunneling microscope-based break-junction technique to compare the single-molecule conductance of these oligosilanes to those of alkanes. We found that the molecular conductance decreases exponentially with increasing chain length with a decay constant β = 0.27 ± 0.01 A-1, comparable to that of a conjugated chain of C = C π bonds. This result demonstrates the profound implications of σ conjugation for the conductivity of silicon.

Synthesis of dichloro derivatives of linear and cyclic permethyloligosilanes and cyclolinear permethylpolysilane-siloxanes and permethylpolyoxysilane based on them

Chernyavskii, A. I.,Larkin, D. Yu.,Chernyavskaya, N. A.

, p. 175 - 180 (2007/10/03)

The reactions of dodecamethylcyclohexasilane with chlorides of I, II, IV-VI, and VIII Group metals were studied as a promising approach to the synthesis of functional oligosilanes. When cyclohexasilane reacts with metal chlorides without a solvent at elevated temperatures, the process is intensified and, in some cases, the selectivity of formation of chloro derivatives of linear and cyclic permethyloligosilanes increases. The cyclolinear permethylpolysilane-siloxanes were prepared by heterofunctional polycondensation of the resulting oligosilanes with bifunctional cyclic and linear permethyloligosiloxanes. Cyclolinear permethylpolyoxysilane was synthesized for the first time by the reaction of 1,3-dihydroxycyclo-hexasilane with 1,3-dichlorohexamethyltrisilane.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 812-36-2