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342405-19-0

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342405-19-0 Usage

General Description

4-IODO-5-METHYL-1-PHENYL-1H-PYRAZOLE is a chemical compound with the molecular formula C10H9IN2. It is a pyrazole derivative with a phenyl and methyl group attached to the pyrazole ring, as well as an iodine atom at position 4. 4-IODO-5-METHYL-1-PHENYL-1H-PYRAZOLE has been studied for its potential pharmaceutical properties, including its antimicrobial and anti-inflammatory effects. It may also have applications in the development of new drugs and research in the field of organic chemistry. 4-IODO-5-METHYL-1-PHENYL-1H-PYRAZOLE is a valuable chemical for medicinal and chemical research purposes.

Check Digit Verification of cas no

The CAS Registry Mumber 342405-19-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,2,4,0 and 5 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 342405-19:
(8*3)+(7*4)+(6*2)+(5*4)+(4*0)+(3*5)+(2*1)+(1*9)=110
110 % 10 = 0
So 342405-19-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H9IN2/c1-8-10(11)7-12-13(8)9-5-3-2-4-6-9/h2-7H,1H3

342405-19-0SDS

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 4-iodo-5-methyl-1-phenylpyrazole

1.2 Other means of identification

Product number -
Other names 4-Iodo-5-methyl-1-phenyl-1H-pyrazole

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:342405-19-0 SDS

342405-19-0Downstream Products

342405-19-0Relevant articles and documents

Transition-Metal-Free Selective Iodoarylation of Pyrazoles via Heterocyclic Aryliodonium Ylides

Lu, Nannan,Huang, Liangsen,Xie, Lili,Cheng, Jiajia

, p. 3437 - 3443 (2018/07/29)

A one-pot transition-metal-free selective iodoarylation of pyrazoles with aryliodine diacetates has been developed. The reaction proceeds via the generation of NH-pyrazole-iodonium salts in situ, followed by sequential phen/K2CO3-mediated intermolecular arylation. When the iodonium ylide was directly used as substrate, the difunctionalization products could be prepared in high yield under base- and metal-free conditions. This transformation provides an efficient route to high-value multisubstituted pyrazole derivatives from simple and readily available substrates.

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