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85553-52-2

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85553-52-2 Usage

General Description

3-(2-FURYL)BENZALDEHYDE is a chemical compound with a chemical formula of C11H8O2. It is an organic compound that belongs to the class of benzaldehyde derivatives. 3-(2-FURYL)BENZALDEHYDE is a pale yellow, crystalline solid with a sweet, floral odor. It is commonly used as a flavor and fragrance ingredient in the food and cosmetic industries. 3-(2-FURYL)BENZALDEHYDE is also known for its potential medicinal properties and has been studied for its antimicrobial and antioxidant properties. It is important to handle this compound with care as it may cause irritation to the skin, eyes, and respiratory system if not used properly.

Check Digit Verification of cas no

The CAS Registry Mumber 85553-52-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,5,5 and 3 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 85553-52:
(7*8)+(6*5)+(5*5)+(4*5)+(3*3)+(2*5)+(1*2)=152
152 % 10 = 2
So 85553-52-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H8O2/c12-8-9-3-1-4-10(7-9)11-5-2-6-13-11/h1-8H

85553-52-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2-FURYL)BENZALDEHYDE

1.2 Other means of identification

Product number -
Other names 3-Fur-2-ylbenzaldehyde

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:85553-52-2 SDS

85553-52-2Relevant articles and documents

Generation of aryl radicals from arylboronic acids by manganese(III) acetate: Synthesis of biaryls and heterobiaryls

Demir, Ayhan S.,Reis, Oemer,Emrullahoglu, Mustafa

, p. 578 - 580 (2007/10/03)

The efficient generation of aryl radicals from arylboronic acids by manganese(III) acetate is described. In aromatic solvents, in situ generated aryl radicals afford the corresponding biaryls in very good yields. This method works selectively, and yields

Heterocyclic substituted benzyl alcohol, insecticidal ester derivatives, and intermediates

-

, (2008/06/13)

Disclosed and exemplified are insecticidal and acaricidal optionally substituted furylbenzyl, thienylbenzyl, pyrazinylbenzyl, or pyridinzylbenzyl esters of the pyrethroid acids, novel pyrethroid alcohols and other intermediates, and compositions, a method of use and a process for preparation of the esters.

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