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1,4,4-Trimethyl-1-cycloheptene is a cyclic hydrocarbon compound with the molecular formula C10H18. It features a seven-membered carbon ring structure, with three methyl groups attached to the first, fourth, and fourth carbon atoms, respectively. This organic compound is an alkene, characterized by the presence of a carbon-carbon double bond, which is located between the first and second carbon atoms in the ring. 1,4,4-Trimethyl-1-cycloheptene is a colorless liquid with a pungent odor and is insoluble in water. It is used as a chemical intermediate in the synthesis of various organic compounds and can be found in trace amounts in some essential oils. Due to its reactivity, it is important to handle 1,4,4-Trimethyl-1-cycloheptene. with care, as it may undergo addition reactions with various reagents, such as halogens and hydrogen halides.

4755-36-6

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4755-36-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4755-36-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,5 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4755-36:
(6*4)+(5*7)+(4*5)+(3*5)+(2*3)+(1*6)=106
106 % 10 = 6
So 4755-36-6 is a valid CAS Registry Number.

4755-36-6SDS

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 1,4,4-trimethylcycloheptene

1.2 Other means of identification

Product number -
Other names 1,4,4-Trimethyl-cyclohepten

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:4755-36-6 SDS

4755-36-6Downstream Products

4755-36-6Relevant academic research and scientific papers

DISPROPORTIONATION OF HYDROGEN IN 3-CARENE

Manukov, E. N.,Chuiko, V. A.,Vyglazov, O. G.

, p. 257 - 262 (2007/10/02)

The disproportionation of hydrogen in 3-carene takes place with the formation of compounds of the 1,1,4-trimethylcycloheptane series.The proposed reaction mechanism involves dehydration of the 2-carene to 2,4-caradiene, which exists in a rapid tautomeric equilibrium with 3,7,7-trimethyl-1,3,5-cycloheptatriene.This gives rise to the appearance of compounds with a seven-membered ring in the reaction product.

HETEROGENEOUS HYDROGENATION OF 3,7,7-TRIMETHYLCYCLOHEPTA-1,3,5-TRIENE

Manukov, E. N.,Chuiko, V. A.

, p. 422 - 425 (2007/10/02)

It has been shown that the intermediate products of the hydrogenation of 3,7,7-trimethylcyclohepta-1,3,5-triene on platinum black are 2- and 3-carenes, in addition to olefins and dienes of the 1,1,4-trimethylcycloheptane series.The final hydrogenation products contains 96percent of 1,1,4-trimethylcycloheptane and 4percent of carenes.

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