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27466-83-7

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27466-83-7 Usage

General Description

4-Bromo-N-methylbenzamide 98% is a chemical compound with the molecular formula C8H8BrNO. It is a white solid with a purity of 98% and is commonly used in research and industrial applications. 4-Bromo-N-methylbenzamide 98% is a derivative of N-methylbenzamide with an added bromine atom, and it is often utilized as a building block in organic synthesis. Due to its high purity, 4-Bromo-N-methylbenzamide 98% is favored in laboratory settings for its reliability and consistency in reactions. It is important to handle this chemical with caution and in accordance with safety guidelines, as it may pose potential health hazards if not handled properly.

Check Digit Verification of cas no

The CAS Registry Mumber 27466-83-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,4,6 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 27466-83:
(7*2)+(6*7)+(5*4)+(4*6)+(3*6)+(2*8)+(1*3)=137
137 % 10 = 7
So 27466-83-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H8BrNO/c1-10-8(11)6-2-4-7(9)5-3-6/h2-5H,1H3,(H,10,11)

27466-83-7 Well-known Company Product Price

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  • Alfa Aesar

  • (H57940)  4-Bromo-N-methylbenzamide, 97%   

  • 27466-83-7

  • 250mg

  • 990.0CNY

  • Detail
  • Alfa Aesar

  • (H57940)  4-Bromo-N-methylbenzamide, 97%   

  • 27466-83-7

  • 1g

  • 3175.0CNY

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27466-83-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-bromo-N-methylbenzamide

1.2 Other means of identification

Product number -
Other names p-bromo-N-methylbenzamide

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:27466-83-7 SDS

27466-83-7Relevant articles and documents

Assemblies of 1,4-Bis(diarylamino)naphthalenes and Aromatic Amphiphiles: Highly Reducing Photoredox Catalysis in Water

Abe, Manabu,Akita, Munetaka,Chitose, Youhei,Hyodo, Yuki,Koike, Takashi,Takahashi, Keigo,Yoshizawa, Michito

supporting information, (2021/10/21)

Host-guest assemblies of a designed 1,4-bis(diarylamino)naphthalene and V-shaped aromatic amphiphiles consisting of two pentamethylbenzene moieties bridged by an m -phenylene unit bearing two hydrophilic side chains emerged as highly reducing photoredox catalysis systems in water. An efficient demethoxylative hydrogen transfer of Weinreb amides has been developed. The present supramolecular strategy permits facile tuning of visible-light photoredox catalysis in water.

The Pd-catalyzed synthesis of difluoroethyl and difluorovinyl compounds with a chlorodifluoroethyl iodonium salt (CDFI)

Cao, Chengyao Kimmy,Chen, Chao,Ge, Chenxin,Niu, Yaru,Qu, Hongmei

supporting information, (2021/10/01)

Herein, we report a simple and efficient method for the direct installation of chlorodifluoroethyl group onto aromatic molecules of various aromatic amides with a new 2-chloro,2,2-difluoroethyl(mesityl)iodonium salt (CDFI). Moreover, the chlorodifluoroeth

N2-carbamylaryl-2-aminopyrimidine derivative and medical application thereof

-

Paragraph 0037; 0040-0041; 0102-0104, (2020/10/28)

The invention provides an N2-carbamylaryl-2-aminopyrimidine derivative and a medical application thereof. The N2-carbamylaryl-2-aminopyrimidine derivative provided by the invention comprises an optical isomer of the N2-carbamylaryl-2-aminopyrimidine derivative and pharmaceutically acceptable salt thereof. Pharmacodynamic research shows that the traditional Chinese medicine composition has no toxicor side effect, the compound has an FLT3 inhibitory activity. The proliferation inhibition activity is realized on various leukemia cell strains; a medium inhibition effect is achieved on breast cancer cells; moreover, the polypeptide is effective for multiple mutations of AML, such as internal tandem repeat mutation of a near-membrane structural domain and D835 point mutation of an activated ring in a kinase structural domain, almost has no inhibition effect on c-KIT, can overcome drug resistance brought by clinical point mutation, can reduce toxic and side effects of bone marrow inhibition,and can be applied to preparation of antitumor drugs. The structures of the general formulas Ia and Ib of the N2-carbamylaryl-2-aminopyrimidine derivative are shown in the specification,

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