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1,5-di(furan-2-yl)pentan-3-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79461-31-7

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79461-31-7 Usage

Derivative of

Furan (a heterocyclic compound)

Structural feature

Long carbon chain with two furan rings attached

Applications

a. Organic synthesis
b. Pharmaceuticals
c. Flavorings
d. Perfumes

Potential

a. Biological activity
b. Pharmacological properties

Functional group

Pentan-3-ol (alcohol-like properties)

Solubility

Likely soluble in water due to the presence of the pentan-3-ol group

Interactions

Capable of interacting with other organic molecules due to the alcohol-like properties of the pentan-3-ol group

Versatility

Wide range of uses and potential implications in various fields, including pharmaceuticals, flavorings, and perfumes

Further research

May be studied for its potential pharmacological properties and biological activity

Check Digit Verification of cas no

The CAS Registry Mumber 79461-31-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,4,6 and 1 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 79461-31:
(7*7)+(6*9)+(5*4)+(4*6)+(3*1)+(2*3)+(1*1)=157
157 % 10 = 7
So 79461-31-7 is a valid CAS Registry Number.

79461-31-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,5-bis(furan-2-yl)pentan-3-ol

1.2 Other means of identification

Product number -
Other names 2-Furanpropanol,a-[2-(2-furanyl)ethyl]

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:79461-31-7 SDS

79461-31-7Relevant academic research and scientific papers

EFFECT OF THE NATURE OF THE SOLVENT ON THE RATE AND MECHANISM OF THE CATALYTIC HYDROGENATION OF DIFURFURYLIDENEACETONE

Mat'yakubov, R.,Mamatov, Yu. M.

, p. 651 - 655 (2007/10/02)

It was established that the hydrogenation of difurfurylideneacetone on a skeletal Ni-Ti-Al catalyst at atmospheric pressure proceeds nonselectively.The rate of hydrogenation in both aprotic and protic solvents increases as their overall electrophilicity increases.The process is realized selectively under hydrogen pressure.By changing the type of solvent one can obtain a catalyzate enriched in various reaction products.

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