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638-04-0

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638-04-0 Usage

Description

CIS-1,3-DIMETHYLCYCLOHEXANE is a variation of volatile organic compounds (VOCs) that can be found in the breath of normal humans. It is a chemical compound with the molecular formula C8H16 and is characterized by its cyclic structure and the presence of two methyl groups attached to the first and third carbon atoms.

Uses

Used in Medical Applications:
CIS-1,3-DIMETHYLCYCLOHEXANE is used as a biomarker in medical applications for monitoring the presence of certain diseases or conditions. The detection of this compound in breath samples can provide valuable information about a person's health and help in the diagnosis and management of various medical conditions.
Used in Environmental Applications:
CIS-1,3-DIMETHYLCYCLOHEXANE is also used in environmental applications for monitoring air quality and assessing the presence of pollutants. The analysis of this compound in air samples can help in identifying the sources of pollution and implementing measures to improve air quality.
Used in Industrial Applications:
CIS-1,3-DIMETHYLCYCLOHEXANE is used as a raw material or intermediate in the synthesis of various chemicals and materials in the chemical industry. Its unique chemical properties make it suitable for use in the production of solvents, fragrances, and other specialty chemicals.
Used in Research Applications:
CIS-1,3-DIMETHYLCYCLOHEXANE is used as a research compound in scientific studies to investigate its properties, reactions, and potential applications. Researchers can use this compound to explore new chemical reactions, develop new synthetic methods, and gain insights into the structure and behavior of similar compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 638-04-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,3 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 638-04:
(5*6)+(4*3)+(3*8)+(2*0)+(1*4)=70
70 % 10 = 0
So 638-04-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H16/c1-7-4-3-5-8(2)6-7/h7-8H,3-6H2,1-2H3/t7-,8+

638-04-0 Well-known Company Product Price

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  • Aldrich

  • (118362)  cis-1,3-Dimethylcyclohexane  99%

  • 638-04-0

  • 118362-5G

  • 1,065.87CNY

  • Detail

638-04-0SDS

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 CIS-1,3-DIMETHYLCYCLOHEXANE

1.2 Other means of identification

Product number -
Other names 1,3-Dimethyl-cyclohexan

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:638-04-0 SDS

638-04-0Relevant articles and documents

Deno et al.

, p. 1744 (1964)

One-pot dual catalysis for the hydrogenation of heteroarenes and arenes

Chatterjee, Basujit,Kalsi, Deepti,Kaithal, Akash,Bordet, Alexis,Leitner, Walter,Gunanathan, Chidambaram

, p. 5163 - 5170 (2020/09/07)

A simple dinuclear monohydrido bridged ruthenium complex [{(η6-p-cymene)RuCl}2(μ-H-μ-Cl)] acts as an efficient and selective catalyst for the hydrogenation of various heteroarenes and arenes. The nature of the catalytically active species was investigated using a combination of techniques including in situ reaction monitoring, kinetic studies, quantitative poisoning experiments and electron microscopy, evidencing a dual reactivity. The results suggest that the hydrogenation of heteroarenes proceeds via molecular catalysis. In particular, monitoring the reaction progress by NMR spectroscopy indicates that [{(η6-p-cymene)RuCl}2(μ-H-μ-Cl)] is transformed into monomeric ruthenium intermediates, which upon subsequent activation of dihydrogen and hydride transfer accomplish the hydrogenation of heteroarenes under homogeneous conditions. In contrast, carbocyclic aryl motifs are hydrogenated via a heterogeneous pathway, by in situ generated ruthenium nanoparticles. Remarkably, these hydrogenation reactions can be performed using molecular hydrogen under solvent-free conditions or with 1,4-dioxane, and thus give access to a broad range of saturated heterocycles and carbocycles while generating no waste.

Effects of steam on toluene hydrogenation over a Ni catalyst

Atsumi, Ryosuke,Kobayashi, Keisuke,Xieli, Cui,Nanba, Tetsuya,Matsumoto, Hideyuki,Matsuda, Keigo,Tsujimura, Taku

, (2019/12/23)

The catalytic toluene hydrogenation over Ni/SiO2 was carried out using H2 or a H2/H2O mixture. The toluene conversion and MCH selectivity were evaluated under partial steam pressures 0?10 kPa, at H2/t

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