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1592-70-7

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1592-70-7 Usage

Description

4-Vinylbenzylchloride, also known as 4-Vinylbenzyl chloride or α-chloromethylstyrene, is an organic compound with the chemical formula C8H7Cl. It is a colorless liquid with a pungent odor and is used as an intermediate in the synthesis of various chemicals and materials. It possesses a vinyl group and a benzyl chloride group, which allows for further chemical reactions and modifications.

Uses

Used in Chemical Synthesis:
4-Vinylbenzylchloride is used as a chemical intermediate for the production of various compounds, such as pharmaceuticals, agrochemicals, and other specialty chemicals. Its reactive vinyl and benzyl chloride groups make it a versatile building block in organic synthesis.
Used in Polymer Industry:
In the polymer industry, 4-Vinylbenzylchloride is used as a monomer for the synthesis of polymers with specific properties. The vinyl group can be polymerized to form poly(4-vinylbenzylchloride), which can be further modified or used as a precursor for other polymers with desired characteristics.
Used in Adhesives and Sealants:
4-Vinylbenzylchloride is used as a component in the formulation of adhesives and sealants. Its reactive groups can be involved in the curing process, leading to improved adhesion and sealing properties.
Used in Surface Coatings:
The compound is also used in the development of surface coatings, such as paints and varnishes. Its chemical reactivity allows for the creation of coatings with specific properties, such as improved durability and resistance to environmental factors.
Used in Bioactive Compounds Synthesis:
4-Vinylbenzylchloride can be used in the synthesis of bioactive compounds, such as Isokaempferide, a flavonoid with antioxidant and anticholinesterase activity. Its reactive groups facilitate the formation of complex molecular structures with potential applications in the pharmaceutical and healthcare industries.

Check Digit Verification of cas no

The CAS Registry Mumber 1592-70-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,9 and 2 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1592-70:
(6*1)+(5*5)+(4*9)+(3*2)+(2*7)+(1*0)=87
87 % 10 = 7
So 1592-70-7 is a valid CAS Registry Number.

1592-70-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methoxyapigenin

1.2 Other means of identification

Product number -
Other names 3-methoxy-5,7,4'-trihydroxyflavone

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:1592-70-7 SDS

1592-70-7Relevant articles and documents

Flavonol glycosides from Centaurea furfuracea. Antiplasmodial and cytotoxic activities

Akkal,Benayache,Medjroubi,Tillequin

, p. 319 - 320 (2007)

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4'-Hydroxy-3-methoxyflavones with potent antipicornavirus activity

De Meyer,Haemers,Mishra,Pandey,Pieters,Vanden Berghe,Vlietinck

, p. 736 - 746 (2007/10/02)

4'-Hydroxy-3-methoxyflavones are natural compounds with known antiviral activities against picornaviruses such as poliomyelitis and rhinoviruses. In order to establish a structure-activity relationship a series of analogues were synthesized, and their antiviral activities and cytotoxicities were compared with those of flavones from natural origin. The 4'-hydroxyl and 3-methoxyl groups, a substitution in the 5 position and a polysubstituted A ring appeared to be essential requirements for a high activity. The most interesting compound was 4',7-dihydroxy-3-methoxy-5,6-dimethylflavone possessing in vitro TI99 values of > 1000 and > 200 against poliovirus type 1 and rhinovirus type 15, respectively. This compound was also active against other rhinovirus serotypes (2, 9, 14, 29, 39, 41, 59, 63, 70, 85, and 89) tested, having MIC50 values ranging from 0.016 to 0.5 μg/mL. Finally in contrast to quercetin it showed to be not mutagenic in concentrations up to 2.5 mg in the Ames test.

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