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1-(3-bromophenyl)-5-methyl-1H-pyrazole-3-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

784142-83-2

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784142-83-2 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 10 carbon (C), 9 hydrogen (H), 1 bromine (Br), 4 nitrogen (N), and 1 oxygen (O) atoms.

Explanation

Pyrazole derivatives are a class of organic compounds containing a five-membered heterocyclic ring with two nitrogen atoms. 1-(3-bromophenyl)-5-methyl-1H-pyrazole-3-carboxamide belongs to this class.

Explanation

The compound contains a bromophenyl group, which is a phenyl ring (a six-membered carbon ring with alternating single and double bonds) with a bromine atom attached to the third carbon.

Explanation

The carboxamide group is a functional group consisting of a carbonyl group (C=O) attached to an amine group (-NH2). In 1-(3-bromophenyl)-5-methyl-1H-pyrazole-3-carboxamide, the carboxamide group is connected to the pyrazole ring.

Explanation

A methyl group (-CH3) is a single carbon atom bonded to three hydrogen atoms. In 1-(3-bromophenyl)-5-methyl-1H-pyrazole-3-carboxamide, a methyl substituent is attached to the pyrazole ring, which adds steric bulk and can influence the compound's properties.

Explanation

The pyrazole scaffold is often used in the development of drugs due to its diverse biological activities. This particular compound may have potential uses in the development of new therapeutic agents for treating various diseases and conditions.

Explanation

Pyrazole derivatives, including 1-(3-bromophenyl)-5-methyl-1H-pyrazole-3-carboxamide, are known for their diverse biological activities, which can be exploited in the development of drugs targeting different diseases and conditions.

Explanation

The compound has a heterocyclic structure, meaning it contains a ring of atoms with at least one heteroatom (an atom other than carbon). In this case, the ring is five-membered and contains two nitrogen atoms.

Class

Pyrazole derivative

Bromophenyl group

Attached to the pyrazole ring

Carboxamide group

Present in the molecule

Methyl substituent

Located on the pyrazole ring

Potential applications

Pharmaceutical and medicinal chemistry

Biological activities

Diverse

Structure

Heterocyclic with a five-membered ring

Check Digit Verification of cas no

The CAS Registry Mumber 784142-83-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,8,4,1,4 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 784142-83:
(8*7)+(7*8)+(6*4)+(5*1)+(4*4)+(3*2)+(2*8)+(1*3)=182
182 % 10 = 2
So 784142-83-2 is a valid CAS Registry Number.

784142-83-2SDS

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 1-(3-Bromophenyl)-5-methyl-1H-pyrazole-3-carboxamide

1.2 Other means of identification

Product number -
Other names 1-(3-Bromo-phenyl)-2,5-dihydro-1H-pyrrole

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:784142-83-2 SDS

784142-83-2Downstream Products

784142-83-2Relevant academic research and scientific papers

BIARYL SUBSTITUTED PYRAZOLES AS SODIUM CHANNEL BLOCKERS

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Page 37, (2008/06/13)

Biaryl substituted pyrazole compounds are sodium channel blockers useful for the treatment of pain and other conditions. Pharmaceutical compositions comprise an effective amount of the instant compounds, either alone, or in combination with one or more th

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