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3-Buten-1-ol, 2-methyl, acetate, also known as 2-methyl-3-buten-1-ol acetate or isoamyl acetate, is an organic compound with the chemical formula C7H12O2. It is a colorless liquid with a fruity, banana-like odor and is commonly used as a flavoring agent in the food and beverage industry. This ester is formed by the reaction of 2-methyl-3-buten-1-ol (isopentyl alcohol) with acetic acid, resulting in a compound that contributes to the characteristic aroma of bananas and pears. Isoamyl acetate is also found naturally in various fruits, such as bananas and apples, and is used in the production of artificial fruit flavors, perfumes, and as a solvent in the pharmaceutical industry.

4806-34-2

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4806-34-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4806-34-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,0 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4806-34:
(6*4)+(5*8)+(4*0)+(3*6)+(2*3)+(1*4)=92
92 % 10 = 2
So 4806-34-2 is a valid CAS Registry Number.

4806-34-2SDS

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-methyl-3-buten-1-yl acetate

1.2 Other means of identification

Product number -
Other names Acetic acid 2-methyl-but-3-enyl ester

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:4806-34-2 SDS

4806-34-2Downstream Products

4806-34-2Relevant academic research and scientific papers

The use of metal reagents in stereo- and regioselective functionalizations of conjugated dienes

Baeckval, Jan-E

, p. 665 - 670 (2007/10/02)

Conjugated dienes have been selectively functionalized via 1-acetoxy-4-chloro-2-alkenes and via 2-(phenylsulfonyl)-1,3-dienes.In both these approaches nucleophiles can be added to the 1- and 4-positions.It was shown that also non-stabilized carbon nucleophiles (from cuprates or copper(I)-catalyzed Grignard reactions) can be used.The utility of the functionalizations was demonstrated by the syntheses of a marine natural product and a butterfly pheromone.Finally, the 2-(phenyl-sulfonyl)-1,3-dienes show a dual electron demand in Diels-Alder reactions and give cycloadducts with both electron-rich and electron-deficient olefins.

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