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2-(3-methylbutyl)tetrahydrofuran is a cyclic organic compound with the molecular formula C9H18O. It is a derivative of tetrahydrofuran, a saturated heterocyclic compound consisting of a four-membered ring with one oxygen atom and three carbon atoms. The 2-(3-methylbutyl)tetrahydrofuran features a 3-methylbutyl group attached to the 2-position of the tetrahydrofuran ring. This alkyl chain consists of a four-carbon chain with a methyl group attached to the third carbon. The compound is known for its unique chemical properties and potential applications in various industries, such as pharmaceuticals and fragrances, due to its distinct structure and functional groups.

2429-95-0

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2429-95-0 Usage

Physical state

Colorless liquid

Odor

Fruity, earthy

Common uses

Solvent in industrial applications (production of coatings, adhesives, and specialty chemicals), fragrance ingredient in perfumes and personal care products

Notable properties

High solvency power, compatibility with a wide range of substances

Safety concerns

Flammability, potential health hazards if not used properly

Check Digit Verification of cas no

The CAS Registry Mumber 2429-95-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,2 and 9 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2429-95:
(6*2)+(5*4)+(4*2)+(3*9)+(2*9)+(1*5)=90
90 % 10 = 0
So 2429-95-0 is a valid CAS Registry Number.

2429-95-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-Methylbutyl)tetrahydrofur

1.2 Other means of identification

Product number -
Other names 2-isopentyltetrahydrofuran

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:2429-95-0 SDS

2429-95-0Downstream Products

2429-95-0Relevant academic research and scientific papers

SELECTIVITY OF TETRAHYDROFURAN FORMATION FROM UNACTIVATED ALIPHATIC ALCOHOLS BY THE BROMINE-SILVER-SALT REACTION

Roscher, Nina Matheny,Shaffer, D. Kent

, p. 2643 - 2650 (2007/10/02)

Studies of the bromine-silver carbonate reaction with aliphatic alcohols in which intramolecular δ-H competition is possible are generally quite specific.Loss of a tertiary δ- hydrogen occurs preferentially from both tertiary and secondary aliphatic alcohols to yield the most highly substituted cyclic ether.For example, 2,5-dimethyl-2-octanol yields only 2,2,5-trimethyl-5-propyltetrahydrofuran as the cyclic ether product; 2-methyl-2-isopentyltetrahydrofuran is not detected.

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