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2896-63-1

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2896-63-1 Usage

General Description

3-propylcatechol, also known as 3-propyl-1,2-dihydroxybenzene, is a chemical compound with the formula C9H12O2. It is a derivative of catechol, a natural phenol found in various plants such as fruits, vegetables, and coffee. 3-propylcatechol is commonly used as a flavoring agent in the food industry due to its sweet, coffee-like aroma. It is also used in the production of fragrances and as a chemical intermediate in the synthesis of pharmaceuticals and other organic compounds. The compound has been studied for its antioxidant and antimicrobial properties, as well as its potential use in the treatment of neurodegenerative diseases. Additionally, 3-propylcatechol has been investigated for its potential role in the development of new materials and biofuels.

Check Digit Verification of cas no

The CAS Registry Mumber 2896-63-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,9 and 6 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2896-63:
(6*2)+(5*8)+(4*9)+(3*6)+(2*6)+(1*3)=121
121 % 10 = 1
So 2896-63-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H12O2/c1-2-4-7-5-3-6-8(10)9(7)11/h3,5-6,10-11H,2,4H2,1H3

2896-63-1SDS

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 3-Propyl-1,2-benzenediol

1.2 Other means of identification

Product number -
Other names 3-propyl-pyrocatechol

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:2896-63-1 SDS

2896-63-1Relevant articles and documents

Synthesis of 3-Alkylcatechols via Intramolecular Cyclization

Miyakoshi, Tetsuo,Togashi, Hiroyasu

, p. 407 - 410 (2007/10/02)

The intramolecular cyclization of 2-alkanoyl-2,5-dimethoxytetrahydrofurans 4 with aqueous acid is described. 3-Alkylcatechols 7 were prepared in generally good yields by boiling the dioxane solution of compounds 4 in the presence of 1 M hydrochloric acid.In addition, 4,5-dioxoalkanals 6 were obtained in good to high yields when the dioxane solution of compounds 4 was treated with 0.1 M hydrochloric acid.

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