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1309597-90-7

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1309597-90-7 Usage

Physical State

Yellowish solid

Uses

a. Production of pharmaceuticals and agrochemicals
b. Development of medicinal products
c. Building block in organic synthesis

Properties

a. Antibacterial
b. Antifungal

Industrial Applications

Wide range of derivatives with potential applications

Hazardous Nature

Potentially hazardous, requires careful handling in laboratory and industrial settings

Check Digit Verification of cas no

The CAS Registry Mumber 1309597-90-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,9,5,9 and 7 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1309597-90:
(9*1)+(8*3)+(7*0)+(6*9)+(5*5)+(4*9)+(3*7)+(2*9)+(1*0)=187
187 % 10 = 7
So 1309597-90-7 is a valid CAS Registry Number.

1309597-90-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-chloro-5-naphthalen-2-ylthiophen-2-yl)ethanone

1.2 Other means of identification

Product number -
Other names 1-(4-Chloro-5-(naphthalen-2-yl)thiophen-2-yl)ethan-1-one

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:1309597-90-7 SDS

1309597-90-7Downstream Products

1309597-90-7Relevant articles and documents

Palladium-catalyzed direct 5-arylation of formyl- or acetyl-halothiophene derivatives

Beydoun, Kassem,Doucet, Henri

experimental part, p. 1749 - 1759 (2011/05/14)

Pd(OAc)2 was found to catalyze the direct arylation of some functionalized halothiophene derivatives allowing the synthesis in only one step of polyfunctionalized arylated thiophenes. In the presence of 2-acetyl-3-chlorothiophene, 2-acetyl-4-chlorothiophene, 2-acetyl-3- bromothiophene diethylacetal or 2-(4-bromothiophen-2-yl)-[1,3]dioxolane, and a variety of aryl bromides, the 5-arylation products were obtained in moderate to high yields employing only 0.5 mol% catalyst. On the other hand, the use of 2-formyl-3-chlorothiophene, 2-acetyl-3-bromothiophene or 2-formyl-3- bromothiophene gave disappointing results.

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