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3,3,6,6-Tetramethyl-1,4-cyclohexadiene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

2223-54-3

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2223-54-3 Usage

Synthesis Reference(s)

Tetrahedron Letters, 8, p. 5193, 1967 DOI: 10.1016/S0040-4039(01)89642-8

Check Digit Verification of cas no

The CAS Registry Mumber 2223-54-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,2 and 3 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2223-54:
(6*2)+(5*2)+(4*2)+(3*3)+(2*5)+(1*4)=53
53 % 10 = 3
So 2223-54-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H16/c1-9(2)5-7-10(3,4)8-6-9/h5-8H,1-4H3

2223-54-3SDS

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 3,3,6,6-tetramethylcyclohexa-1,4-diene

1.2 Other means of identification

Product number -
Other names 3,3,6,6-tetramethyl-cyclohexa-1,4-diene

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:2223-54-3 SDS

2223-54-3Relevant academic research and scientific papers

Reaktionen der Cyclopropene, V. Cyclooligomerisierungen von 3,3-Dialkylcyclopropenen an Palladium(0)-Katalysatoren

Binger, Paul,Schuchardt, Ulf

, p. 1649 - 1655 (2007/10/02)

At phosphane free palladium(0) catalysts 3,3-dialkylcyclopropenes hept-1-ene (4)> are cyclooligomerised to give the trans-tricyclo2,4>hexane derivatives 6, 7, and 8, and the pentacyclo2,4.05,7.08,10>dodecane derivatives 10, 11, and 12.Contrary to this at triisopropylphosphane modified palladium(0) catalysts the tetracyclo2,4.05,7>nonane derivatives 14, 15, and 16 are formed selectively in more than 80percent yield.

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