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4-(4-Methylpiperazinomethyl)benzophenone is a chemical compound that belongs to the class of compounds known as benzophenones. It is characterized by a combination of two aromatic rings and a ketone functional group, with a sub-classification as an organopiperazine due to the presence of a piperazine moiety carrying an alkyl group. 4-(4-METHYLPIPERAZINOMETHYL)BENZOPHENONE is potentially reactive and must be handled with caution. Its properties, reactions, and uses may vary depending on the specific conditions and requirements of its applications.

898783-42-1

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898783-42-1 Usage

Uses

Used in Pharmaceutical Industry:
4-(4-Methylpiperazinomethyl)benzophenone is used as an intermediate in the manufacturing of pharmaceuticals for its potential reactivity and structural characteristics that can be utilized in the synthesis of various drug compounds.
Used in Organic Compounds Synthesis:
In the chemical industry, 4-(4-Methylpiperazinomethyl)benzophenone serves as an intermediate in the synthesis of organic compounds, leveraging its unique structure to form a variety of products with different applications.

Check Digit Verification of cas no

The CAS Registry Mumber 898783-42-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,8,7,8 and 3 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 898783-42:
(8*8)+(7*9)+(6*8)+(5*7)+(4*8)+(3*3)+(2*4)+(1*2)=261
261 % 10 = 1
So 898783-42-1 is a valid CAS Registry Number.
InChI:InChI=1/C19H22N2O/c1-20-11-13-21(14-12-20)15-16-7-9-18(10-8-16)19(22)17-5-3-2-4-6-17/h2-10H,11-15H2,1H3

898783-42-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-[(4-methylpiperazin-1-yl)methyl]phenyl]-phenylmethanone

1.2 Other means of identification

Product number -
Other names 4-(4-METHYLPIPERAZIN-1-YLMETHYL)BENZOPHENONE

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:898783-42-1 SDS

898783-42-1Downstream Products

898783-42-1Relevant articles and documents

Aminomethylation via cyclopalladated-ferrocenylimine-complexes-catalyzed Suzuki-Miyaura coupling of aryl halides with potassium N, N - dialkylaminomethyltrifluoroborates

Zou, Dapeng,Cui, Hongmeng,Qin, Lijin,Li, Jingya,Wu, Yangjie,Wu, Yusheng

scheme or table, p. 349 - 356 (2011/03/23)

Using cyclopalladated ferrocenylimine complexes (1-3 mol%) as catalysts, the Suzuki-Miyaura coupling of potassium N,N-dialkylaminomethyltrifluoroborates with aryl and heteroaryl halides were carried out in a 10:1 THF-H2O mixture at 80° in the presence of Cs2CO3 (3.0 equiv) as base, giving the desired cross-coupling products in 14-87% yields. A variety of potassium alkyltrifluoroborates were also examined. Georg Thieme Verlag Stuttgart New York.

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