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30148-18-6

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30148-18-6 Usage

General Description

(4-CHLOROPHENYL)(1-METHYL-1H-IMIDAZOL-2-YL)METHANONE is a chemical compound that belongs to the class of benzophenones. It consists of a chlorophenyl group and a 1-methyl-1H-imidazol-2-yl group connected to a methanone functional group. (4-CHLOROPHENYL)(1-METHYL-1H-IMIDAZOL-2-YL)METHANONE is often used in pharmaceutical research and drug development due to its potential as a pharmacological agent. It may also have applications in the fields of organic synthesis and medicinal chemistry. The exact properties and uses of this chemical may vary depending on the specific research or application context.

Check Digit Verification of cas no

The CAS Registry Mumber 30148-18-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,1,4 and 8 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 30148-18:
(7*3)+(6*0)+(5*1)+(4*4)+(3*8)+(2*1)+(1*8)=76
76 % 10 = 6
So 30148-18-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H9ClN2O/c1-14-7-6-13-11(14)10(15)8-2-4-9(12)5-3-8/h2-7H,1H3

30148-18-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-Chlorophenyl)(1-methyl-1H-imidazol-2-yl)methanone

1.2 Other means of identification

Product number -
Other names 2-(4-chlorobenzoyl)-1,3,5-trimethyl-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:30148-18-6 SDS

30148-18-6Relevant articles and documents

Facile preparation of aromatic ketones from aromatic bromides and arenes with aldehydes

Ushijima, Sousuke,Dohi, Souya,Moriyama, Katsuhiko,Togo, Hideo

scheme or table, p. 1436 - 1442 (2012/03/09)

Aromatic ketones were efficiently prepared in good yields by the reactions of aryl bromides with n-BuLi, followed by the reactions with aromatic aldehydes or aliphatic aldehydes and the subsequent treatment with molecular iodine and K2CO3, in a one-pot method. The same treatment of arenes, instead of aromatic bromides, also provided the corresponding aromatic ketones in good yields. Using these methods, various diaryl ketones and alkyl aryl ketones bearing electron-rich aromatics and electron-deficient aromatics could be prepared efficiently by a simple, transition-metal-free, and therefore environmentally benign experimental procedure.

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