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1,2-diethenylcyclobutane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

2422-85-7

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2422-85-7 Usage

Type of compound

Organic compound

Structure

Cyclic hydrocarbon with a four-membered ring

Attached groups

Two ethenyl (vinyl) groups attached to adjacent carbon atoms

Uses

Building block in organic synthesis, production of pharmaceuticals and specialty chemicals

Reactivity

Highly reactive due to the presence of double bonds

Reaction types

Can undergo addition, oxidation, and reduction reactions

Safety precautions

Handle with caution, flammable, may cause skin and eye irritation

Check Digit Verification of cas no

The CAS Registry Mumber 2422-85-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,2 and 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2422-85:
(6*2)+(5*4)+(4*2)+(3*2)+(2*8)+(1*5)=67
67 % 10 = 7
So 2422-85-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H12/c1-3-7-5-6-8(7)4-2/h3-4,7-8H,1-2,5-6H2

2422-85-7SDS

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 (Z)-1,2-Divinylcyclobutan

1.2 Other means of identification

Product number -
Other names 1,2-divinylcyclobutane

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:2422-85-7 SDS

2422-85-7Downstream Products

2422-85-7Relevant academic research and scientific papers

Liquid-phase cyclodimerization of 1,3-butadiene in a closed batch system

Sun, Daolai,Sato, Fumiya,Yamauchi, Shin-Ichi,Yamada, Yasuhiro,Sato, Satoshi

, p. 529 - 533 (2013/05/23)

Dimerization of 1,3-butadiene was investigated in a closed batch system under high-pressure conditions. 4-Vinylcyclohexene was mainly produced without using any solvents or catalysts at temperatures of 150215 °C. The conversion of 1,3-butadiene was signif

Photoelimination of nitrogen from cyclic azo alkanes. An exceptionally labile and an exceptionally reluctant diazabicyclo[2.2.2]octene

Turro, Nicholas J.,Liu, Jonq-Min,Martin, Hans-Dieter,Kunze, Michael

, p. 1299 - 1302 (2007/10/02)

The photochemistry of an unusually reactive diazabicyclo[2.2.2]octene has been found to be extremely solvent and temperature dependent; an exceptionally stable diazabicyclo[2.2.2]octene has been found to undergo a novel fragmentation as a result of vapor phase photoexcitation.

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