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1-Benzyl-5-broMo-1H-pyrazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

145162-70-5

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145162-70-5 Usage

Classification

Brominated pyrazole derivative

Usage

Medicinal and pharmaceutical research

Potential Properties

Anti-cancer, antitumor

Possible Applications

Development of new drugs

Additional Research

Pesticide and insecticide development

Insecticidal Activity

Present

Versatility

High, with various potential applications

Research Interest

Attracts researchers from different fields

Check Digit Verification of cas no

The CAS Registry Mumber 145162-70-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,1,6 and 2 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 145162-70:
(8*1)+(7*4)+(6*5)+(5*1)+(4*6)+(3*2)+(2*7)+(1*0)=115
115 % 10 = 5
So 145162-70-5 is a valid CAS Registry Number.

145162-70-5SDS

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 1-benzyl-5-bromopyrazole

1.2 Other means of identification

Product number -
Other names 1-Benzyl-5-bromo-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:145162-70-5 SDS

145162-70-5Downstream Products

145162-70-5Relevant academic research and scientific papers

HETEROARYL SUBSTITUTED 3-(1-OXOISOINDOLIN-2-YL)PIPERIDINE-2,6-DIONE DERIVATIVES AND USES THEREOF

-

Page/Page column 315, (2022/02/15)

The present disclosure provides a compound of Formula (I): (I), or a pharmaceutically acceptable salt, hydrate, solvate, prodrug, stereoisomer, or tautomer thereof, wherein Rx and X1 are as defined herein, and methods of making and using same.

PYRAZOLE DERIVATIVES AS PHOSPHODIESTERASE 4 INHIBITORS

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Page 137, (2008/06/13)

Selective PDE4 inhibition is achieved by aryl and heteroaryl pyrazole compounds. The compounds exhibit improved PDE4 inhibition as compared to compounds such as rolipram and show selectivity with regard to inhibition of other classes of PDEs.

Synthesis of 2-Alkylpyrazole-1-oxides: A Facile Access to 1-Alkyl-5-halopyrazoles

Eskildsen, Joergen,Vedsoe, Per,Begtrup, Mikael

, p. 1053 - 1056 (2007/10/03)

Selective N-alkylation of 1-hydroxypyrazole 1 into the corresponding 2-alkyl-pyrazole-1-oxides 2a-f has been achieved by treatment with alkyl bromides in the absence of base. Subsequent deoxygenation/halogenation into 1-alkyl-5-halopyrazoles 3a-d and 4a-d using phosphorus oxyhalides is described.

2-Substituted Pyrazole 1-Oxides. Preparation and Reaction with Electrophilic Reagents

Begtrup, Mikael,Larsen, Peter,Vedsoe, Per

, p. 972 - 980 (2007/10/02)

1-Substituted pyrazoles have been oxidized by peracids to 2-substituted pyrazole 1-oxides.This leads to a change in reactivity towards electrophilic attack. 2-Benzylpyrazole 1-oxide is brominated, chlorinated, and nitrated selectively at C-3.The 3-halo-su

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