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135005-24-2

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135005-24-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 135005-24-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,0,0 and 5 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 135005-24:
(8*1)+(7*3)+(6*5)+(5*0)+(4*0)+(3*5)+(2*2)+(1*4)=82
82 % 10 = 2
So 135005-24-2 is a valid CAS Registry Number.

135005-24-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-ethenylphenyl)ethynyl-trimethylsilane

1.2 Other means of identification

Product number -
Other names Silane,[(4-ethenylphenyl)ethynyl]trimethyl

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:135005-24-2 SDS

135005-24-2Relevant articles and documents

Synthesis of Enantiopure C3-Symmetric Triangular Molecules

Miura, Tomoya,Nakamuro, Takayuki,Stewart, Scott G.,Nagata, Yuuya,Murakami, Masahiro

, p. 3334 - 3338 (2017)

An asymmetric synthesis of C3-symmetric triangular macrocycles is reported. 1-Methylsulfonyl-4-(4-vinylphenyl)-1,2,3-triazole undergoes a rhodium(II)-catalyzed cyclotrimerization to establish an enantiopure C3-symmetric triangular ma

Zinc-Catalysed Hydroboration of Terminal and Internal Alkynes

Mandal, Souvik,Mandal, Sayantan,Geetharani

, p. 4553 - 4556 (2019/08/20)

A regioselective hydroboration of alkynes has been developed by using commercially available zinc triflate as a catalyst, in the presence of catalytic amount of NaBHEt3. The reaction tolerates a wide range of terminal alkynes having several synthetically useful functional groups and proceeds regioselectively to furnish hydroborated products in moderate to excellent yields. This system shows moderate chemoselectivity towards terminal C≡C bond over terminal and internal C=C bond and internal C≡C bond.

Palladium catalysed regio- and stereoselective synthesis of (E)-4-aryl-1,3-bis(trimethylsilyl)but-3-en-1-ynes

Rogalski, Szymon,Kubicki, Maciej,Pietraszuk, Cezary

, p. 6192 - 6198 (2018/09/17)

A practical and general synthetic approach to a series of 4-aryl-but-3-en-1-ynes is described. In the presence of palladium complexes a variety of aryl bromides (or iodides) undergo coupling with two equivalents of trimethylsilylacetylene with the formati

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