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N-Hexadecylcyclohexane is a chemical compound with the molecular formula C24H48. It is a cyclic alkane with a hexadecyl (C16H33) alkyl chain attached to the cyclohexane ring. N-HEXADECYLCYCLOHEXANE is an organic molecule that belongs to the class of alkanes, characterized by the presence of only single bonds between carbon atoms. N-Hexadecylcyclohexane is a colorless, odorless, and non-polar liquid with a high boiling point due to its large molecular size and the presence of a cyclic structure. It is insoluble in water but soluble in organic solvents such as hexane, toluene, and chloroform. N-HEXADECYLCYCLOHEXANE has potential applications in various industries, including pharmaceuticals, cosmetics, and as a component in the synthesis of other organic compounds.

6812-38-0

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6812-38-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6812-38-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,1 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6812-38:
(6*6)+(5*8)+(4*1)+(3*2)+(2*3)+(1*8)=100
100 % 10 = 0
So 6812-38-0 is a valid CAS Registry Number.
InChI:InChI=1/C22H44/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-16-19-22-20-17-15-18-21-22/h22H,2-21H2,1H3

6812-38-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Hexadecylcyclohexane

1.2 Other means of identification

Product number -
Other names Cyclohexane, hexadecyl-

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:6812-38-0 SDS

6812-38-0Downstream Products

6812-38-0Relevant academic research and scientific papers

Chloroform as a hydrogen atom donor in barton reductive decarboxylation reactions

Ho, Junming,Zheng, Jingjing,Meana-Paneda, Ruben,Truhlar, Donald G.,Ko, Eun Jung,Savage, G. Paul,Williams, Craig M.,Coote, Michelle L.,Tsanaktsidis, John

, p. 6677 - 6687 (2013/07/26)

The utility of chloroform as both a solvent and a hydrogen atom donor in Barton reductive decarboxylation of a range of carboxylic acids was recently demonstrated (Ko, E. J. et al. Org. Lett. 2011, 13, 1944). In the present work, a combination of electronic structure calculations, direct dynamics calculations, and experimental studies was carried out to investigate how chloroform acts as a hydrogen atom donor in Barton reductive decarboxylations and to determine the scope of this process. The results from this study show that hydrogen atom transfer from chloroform occurs directly under kinetic control and is aided by a combination of polar effects and quantum mechanical tunneling. Chloroform acts as an effective hydrogen atom donor for primary, secondary, and tertiary alkyl radicals, although significant chlorination was also observed with unstrained tertiary carboxylic acids.

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