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4280-89-1

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4280-89-1 Usage

Physical state

Yellowish liquid

Odor

Strong, sweet

Uses

a. Perfumes and flavorings
b. Chemical intermediate in the synthesis of pharmaceuticals and other organic compounds

Chemical properties

a. Ability to form adducts with a variety of nucleophiles
b. Useful in organic synthesis reactions

Biological properties

a. Anti-inflammatory
b. Antitumor

Potential applications

Drug development

Check Digit Verification of cas no

The CAS Registry Mumber 4280-89-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,8 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4280-89:
(6*4)+(5*2)+(4*8)+(3*0)+(2*8)+(1*9)=91
91 % 10 = 1
So 4280-89-1 is a valid CAS Registry Number.

4280-89-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(α-furyl)-5-phenylpenta-1,4-dien-3-one

1.2 Other means of identification

Product number -
Other names 1-[2]Furyl-5-phenyl-penta-1,4-dien-3-on

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:4280-89-1 SDS

4280-89-1Relevant articles and documents

Gram-scale preparation of dialkylideneacetones through Ca(OH)2-catalyzed Claisen-Schmidt condensation in dilute aqueous EtOH

Zhang, Hao,Han, Mengting,Yang, Chenggen,Yu, Lei,Xu, Qing

, (2018/02/06)

A synthetic method of dialkylideneacetones has been developed. Compared with known protocols, the method employed catalytic Ca(OH)2 as the cheap, mild base catalyst and dilute aqueous EtOH (20%, v/v) as the green and safe solvent. The procedure was easily operated: In most cases, the product could be isolated by a simple filtration, and purified by washing with water. This paper provided experimental details of the reactions, which could be applied in gram-scale synthesis and should be a very reliable and practical protocol to prepare these useful compounds in laboratory and at the industrial level.

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