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1-BENZOYL-4-IODOPYRAZOL, a pyrazole derivative with the molecular formula C11H6IN3O, is a chemical compound that features an iodine atom and a benzoyl group. This unique structure and reactivity make it a promising candidate for various applications in organic synthesis and pharmaceutical research. It can serve as a building block in the synthesis of complex organic molecules or as a starting material for developing new drug candidates. Furthermore, its potential biological activities offer opportunities for exploration in medicinal chemistry, highlighting 1-BENZOYL-4-IODOPYRAZOL as a versatile chemical with broad utility in scientific and industrial domains.

116228-38-7

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116228-38-7 Usage

Uses

Used in Organic Synthesis:
1-BENZOYL-4-IODOPYRAZOL is used as a building block for the synthesis of complex organic molecules, leveraging its unique structure and reactivity to facilitate the creation of novel compounds with potential applications in various industries.
Used in Pharmaceutical Research:
1-BENZOYL-4-IODOPYRAZOL is utilized as a starting material in the development of new drug candidates, owing to its potential to contribute to the discovery of innovative therapeutic agents with improved efficacy and selectivity.
Used in Medicinal Chemistry:
1-BENZOYL-4-IODOPYRAZOL is employed for exploring its potential biological activities, which may lead to the identification of new pharmacological targets and the advancement of drug discovery efforts in the field of medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 116228-38-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,2,2 and 8 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 116228-38:
(8*1)+(7*1)+(6*6)+(5*2)+(4*2)+(3*8)+(2*3)+(1*8)=107
107 % 10 = 7
So 116228-38-7 is a valid CAS Registry Number.

116228-38-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-Iodo-1H-pyrazol-1-yl)(phenyl)methanone

1.2 Other means of identification

Product number -
Other names (4-iodopyrazol-1-yl)-phenylmethanone

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:116228-38-7 SDS

116228-38-7Relevant academic research and scientific papers

HETEROCYCLIC COMPOUNDS AS INHIBITORS OF LEUKOTRIENE PRODUCTION

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Paragraph 0343; 0344; 0345; 0346; 0347, (2013/08/14)

The present invention relates to compound of formula (I): or pharmaceutically acceptable salts thereof, wherein R1-R7, A and HET are as defined herein. The invention also relates to pharmaceutical compositions comprising these compounds, methods of using these compounds in the treatment of various diseases and disorders, processes for preparing these compounds and intermediates useful in these processes

FUSED THIOPHENE DERIVATIVES AS KINASE INHIBITORS

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Page/Page column 63, (2008/06/13)

A series of 5,6-dihydro-1-benzothiophen-7(4H)-one derivatives, and analogues thereof, which are substituted in the 2-position by an optionally substituted morpholin-4-yl moiety, being selective inhibitors of PI3 kinase enzymes, are accordingly of benefit in medicine, for example in the treatment of inflammatory, autoimmune, cardiovascular, neurodegenerative, metabolic, oncological, nociceptive or ophthalmic conditions.

On the Chemistry of Pyrazolylalkines; Pyrazoles II.

Heinisch, Gottfried,Holzer, Wolfgang,Obala, Claudia

, p. 253 - 262 (2007/10/02)

Palladium-catalyzed reactions of 1-benzoyl-4-iodopyrazole (2a) with monosubstituted acetylenes 3a,3b and 3c in triethylamine solution provide convenient access to the cross-coupled products 4a,4b and 4c.The 4-ethinylpyrazoles 5a and 7 obtained after metha

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