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2-Butyl-1,1,3-trimethyl-cyclohexane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54676-39-0

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54676-39-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54676-39-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,6,7 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 54676-39:
(7*5)+(6*4)+(5*6)+(4*7)+(3*6)+(2*3)+(1*9)=150
150 % 10 = 0
So 54676-39-0 is a valid CAS Registry Number.

54676-39-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-butyl-1,1,3-trimethylcyclohexane

1.2 Other means of identification

Product number -
Other names Cyclohexane,2-butyl-1,1,3-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:54676-39-0 SDS

54676-39-0Relevant academic research and scientific papers

THE SYNTHESIS OF 1β(H), 6β(Me)-2,2,6-TRIMETHYL-8-ETHYLBICYCLO--7-THIANONANE AND THE STRUCTURE OF THE ISOMERIC BICYCLIC-TERPENOID SULFIDES OCCURRING IN PETROLEUM.

Payzant, J. D.,Cyr, T. D.,Montgomery, D. S.,Strausz, O. P.

, p. 4175 - 4178 (2007/10/02)

The synthesis of the title compound is described.Comparison of ms and nmr data with those of the isomeric bicyclic terpenoid sulfide of petroleum shows that the latter has the structure of 1α(H), 6β(H)-2,2-dimethyl-9-ethylbicyclo--8-thiadecane.

Dehydration Studies of α- and β-Ionol. I With Hexamethylphosphoric Triamide

Whitfield, Frank B.,Sugowdz, Galina

, p. 591 - 600 (2007/10/02)

α-Ionol (2) when heated under reflux with hexamethylphosphoric triamide gave principally one product (1'E)-6-(buta-1',3'-dienyl)-1,5,5-trimethylcyclohex-1-ene (4a) together with trace quantities of the (1'Z)-isomer (4b).Under similar conditions β-Ionol (3) gave as major products (6E,2'E)- and (6Z,2'E)-6-(but-2'-enylidene)-1,5,5-trimethylcyclohex-1-ene (1a) and (1b) together with smaller quantities of (1'E)-1-(buta-1',3'-dienyl)-6,6-dimethyl-2-mehtylenecyclohexane (8) and 1,1,6-trimethyl-1,2,3,4,5,6-hexahydronaphtalene (9).Minor products from this reaction includedthe isomeric trienes (1c) and (1d).Reaction pathways are suggested for the formation of all identified products.

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