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Decahydro-1,2-dimethylnaphthalene is a bicyclic aromatic hydrocarbon with the molecular formula C12H20. It is a derivative of naphthalene, where two hydrogen atoms are replaced by methyl groups, and the molecule is fully saturated, meaning it contains no double bonds. Decahydro-1,2-dimethylnaphthalene is an isomer of decalin, another saturated derivative of naphthalene. Decahydro-1,2-dimethylnaphthalene is a colorless liquid with a boiling point of approximately 210°C and is insoluble in water but soluble in organic solvents. It is used as a solvent, a chemical intermediate in the synthesis of various compounds, and as a component in the production of fuels and lubricants. Due to its chemical structure, it exhibits low toxicity and is considered relatively stable under normal conditions.

3604-14-6

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3604-14-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3604-14-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,0 and 4 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3604-14:
(6*3)+(5*6)+(4*0)+(3*4)+(2*1)+(1*4)=66
66 % 10 = 6
So 3604-14-6 is a valid CAS Registry Number.

3604-14-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-dimethyl-1,2,3,4,4a,5,6,7,8,8a-decahydronaphthalene

1.2 Other means of identification

Product number -
Other names Naphthalene,decahydro-1,2-dimethyl

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:3604-14-6 SDS

3604-14-6Downstream Products

3604-14-6Relevant academic research and scientific papers

Fused-ring alkane fuel and photocatalytic preparation process thereof

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Page/Page column 0027; 0028, (2020/07/05)

A process for preparing a fused-ring alkane fuel, wherein the fused-ring alkane fuel has the following structure: wherein n is 1 or 2; R1, R2, R3, R4 and R5 are H or —CH3 or —CH2CH3; the fused-ring alkane fuel has a density of greater than 0.870 g/cm3, a freezing point of not higher than ?50° C., and a net mass heat value of not less than 42.0 MJ/kg; the process for preparing a fused-ring alkane fuel, wherein the process includes steps of: (1) in a presence of ultraviolet light and a photocatalyst, a Diels-Alder cycloaddition reaction between a substituted or unsubstituted cyclic enone and a substituted or unsubstituted furan molecule occurs to produce a fuel precursor molecule: (2) the fuel precursor molecule obtained in the step (1) is subjected to hydrodeoxygenation to produce the fused-ring alkane fuel.

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