Welcome to LookChem.com Sign In|Join Free

CAS

  • or

18938-24-4

Post Buying Request

18938-24-4 Suppliers

Recommended suppliersmore

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

18938-24-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18938-24-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,9,3 and 8 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 18938-24:
(7*1)+(6*8)+(5*9)+(4*3)+(3*8)+(2*2)+(1*4)=144
144 % 10 = 4
So 18938-24-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H28Si3/c1-12(2,3)10-11(13(4,5)6)14(7,8)9/h10H,1-9H3

18938-24-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-bis(trimethylsilyl)ethenyl-trimethylsilane

1.2 Other means of identification

Product number -
Other names Tris-trimethylsilyl-aethylen

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:18938-24-4 SDS

18938-24-4Downstream Products

18938-24-4Relevant articles and documents

-

Okazaki,R.,Ishii,A.,Inamoto,N.

, p. 279 (1987)

-

Supported gold nanoparticle-catalyzed cis -selective disilylation of terminal alkynes by σ disilanes

Gryparis, Charis,Kidonakis, Marios,Stratakis, Manolis

, p. 6038 - 6041 (2014/01/06)

Supported gold nanoparticles on metal oxides (1 mol %) catalyze for the first time the cis-selective disilylation of terminal alkynes by 1,2-disilanes in isolated yields up to 94%. It is likely that the reaction proceeds through oxidative insertion of the

Episulfone substitution and ring-opening reactions via α-sulfonyl carbanion intermediates

Dishington, Allan P.,Douthwaite, Richard E.,Mortlock, Andrew,Muccioli, Adriano B.,Simpkins, Nigel S.

, p. 323 - 337 (2007/10/03)

Three-membered cyclic sulfones undergo substitution on treatment with base-electrophile mixtures, such as LDA-Me3SiCl and Bu′-P4 phosphazene base-PhCHO, to give either substituted episulfones or the corresponding alkenes following loss of SO2. The structure of a trisilylated episulfone product, 2a, was determined by X-ray crystallography. In the absence of Me3SiCl, reaction of episulfones with lithium diisopropylamide results in ring-opening to give alkenyl sulfinate intermediates, which can be alkylated to give (E)-alkenyl sulfone products in stereoselective fashion.

Platinum-catalyzed elimination-addition reactions of trisilylethenes

Suzuki, Toshio,Lo, Peter Y.

, p. 27 - 33 (2007/10/02)

(E)-1-Hexyldimethylsilyl-1,2-bis(trimethylsilyl)ethene (1) and (E)-1-(3'-butyl-1',3'-tetramethyldisiloxanyl)-1,2-bis(trimethylsilyl)ethene (7) undergo isomerization-redistribution reactions catalyzed by platinum.Each of them is converted into its (Z)-isomer and ethenes bearing one trimethylsilyl group and two substituted silyl groups as major products.The proposed mechanism for the reactions involves a sequence of eliminations of hydrosilanes from the ethenes and re-addition to them.Oxygen greatly affects the reaction apparently accelerating anti-elimination of hydrosilanes.

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 18938-24-4