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Vinylcarborane, also known as 1,2-dicarbollylethylene, is a unique organoborane compound characterized by the presence of two carborane cages (C2B10H12) attached to a vinyl group (C2H3). This molecule exhibits remarkable stability and thermal resistance, with applications in various fields such as polymer chemistry, materials science, and pharmaceuticals. Its structure provides a platform for the development of new materials with enhanced properties, such as heat resistance and chemical stability, making it a promising candidate for advanced technological applications.

20313-28-4

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20313-28-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20313-28-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,3,1 and 3 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 20313-28:
(7*2)+(6*0)+(5*3)+(4*1)+(3*3)+(2*2)+(1*8)=54
54 % 10 = 4
So 20313-28-4 is a valid CAS Registry Number.

20313-28-4SDS

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-vinyl-o-carborane

1.2 Other means of identification

Product number -
Other names 1-ethenyl-o-carborane

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:20313-28-4 SDS

20313-28-4Upstream product

20313-28-4Relevant academic research and scientific papers

o-Carboranylcarbene and m-Carboranylcarbene

Chari, Sarangan L.,Chiang, Sheau-Hwa,Jones, Maitland

, p. 3138 - 3145 (2007/10/02)

Addition of o- and m-carboranylcarbene to olefins takes place in a largely stereospecific fashion.In the addition to cis olefins, it is the anti isomer that predominates.Insertion into carbon-hydrogen bonds occurs with a secondary/primary selectivity ratio of 3.0. (Methyl-o-carboranyl)carbene behaves like tolylcarbene in intramolecular reactions.It yields vinyl-o-carborane and the carborane analogue of benzocyclobutene. (Methyl-m-carboranyl)carbene does not give vinyl-m-carborane.

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