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2-Hexyl-5-methylfuran is an organic compound characterized by a furan ring structure, which is a five-membered aromatic ring containing four carbon atoms and one oxygen atom. This specific derivative features a methyl group (-CH3) at the 5-position and a hexyl chain (-C6H13) at the 2-position, which extends the molecule's structure and influences its properties. It is primarily used as a fragrance compound in the perfumery and flavor industries, imparting a sweet, fruity, and slightly woody aroma. The compound is also of interest in the field of organic synthesis, where it can serve as a building block for more complex molecules. Due to its unique structure and reactivity, 2-hexyl-5-methylfuran has potential applications in the development of pharmaceuticals and other specialty chemicals.

5312-82-3

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5312-82-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5312-82-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,1 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5312-82:
(6*5)+(5*3)+(4*1)+(3*2)+(2*8)+(1*2)=73
73 % 10 = 3
So 5312-82-3 is a valid CAS Registry Number.

5312-82-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hexyl-5-methylfuran

1.2 Other means of identification

Product number -
Other names 1-<5-Methyl-<2>furyl>-hexan

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:5312-82-3 SDS

5312-82-3Relevant academic research and scientific papers

Novel Synthesis of (Z)-3-Hexen-1-ol and cis-Jasmone

Furuhata, Akimichi,Onishi, Ken,Fujita, Akira,Kogami, Kunio

, p. 1757 - 1760 (2007/10/02)

Both (Z)-3-hexen-1-ol and cis-jasmone were synthesised via 1,4-selective hydrogenation of conjugated dienes in the presence of arene Cr(CO)3 or Cr(CO)6 catalysts as the key step.

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