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187805-54-5

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187805-54-5 Usage

General Description

Benzamide, 2-amino-3-fluoro- (9CI) is a chemical compound with the formula C7H7FN2O. It is a fluoro-substituted derivative of benzamide, which is a white solid with a faint odor. Benzamide, 2-amino-3-fluoro- (9CI) is commonly used in organic synthesis and pharmaceutical research due to its potential pharmacological and biological activities. Its specific applications include as a pharmaceutical intermediate and as a building block for the synthesis of various biologically active molecules. Additionally, it has been studied as a potential inhibitor of enzymes and as a source of fluorine in medicinal chemistry. Overall, benzamide, 2-amino-3-fluoro- (9CI) has various potential industrial and research applications.

Check Digit Verification of cas no

The CAS Registry Mumber 187805-54-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,7,8,0 and 5 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 187805-54:
(8*1)+(7*8)+(6*7)+(5*8)+(4*0)+(3*5)+(2*5)+(1*4)=175
175 % 10 = 5
So 187805-54-5 is a valid CAS Registry Number.

187805-54-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Amino-3-fluorobenzamide

1.2 Other means of identification

Product number -
Other names BENZAMIDE,2-AMINO-3-FLUORO

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:187805-54-5 SDS

187805-54-5Downstream Products

187805-54-5Relevant articles and documents

Acid-Catalyzed Synthesis of Isatoic Anhydride-8-Secondary Amides Enables IASA Transformations for Medicinal Chemistry

Gondi, Sudershan R.,Shaik, Althaf,Westover, Kenneth D.

, p. 125 - 136 (2022/01/12)

Quinazolin-dione-N-3-alklyl derivatives are the core scaffolds for several categories of bioactive small molecules, but current synthetic methods are costly, involve environmental hazards, and are not uniformly scalable. Here, we report an inexpensive, flexible, and scalable method for the one-pot synthesis of substituted quinazolin-dione-N-3-alkyls (isomers of isatoic-8-secondary amides (IASAs)) from isatin that take advantage of in situ capture of imidic acid under acidic conditions. We further show that this method can be used for the synthesis of a wide variety of derivatives with medicinal uses.

Oxidative ring-opening of isatins for the synthesis of 2-aminobenzamides and 2-aminobenzoates

Wang, Yu-Wei,Zheng, Lei,Jia, Feng-Cheng,Chen, Yun-Feng,Wu, An-Xin

, p. 1497 - 1503 (2019/02/13)

An efficient and practical isatin-based oxidative domino protocol has been developed for the facile synthesis of 2-aminobenzamides and 2-aminobenzoates. The robust nature of this reaction system is reflected by accessible starting materials, room temperature and high-yield gram-scale synthesis.

POLY-ADP RIBOSE POLYMERASE (PARP) INHIBITORS

-

Page/Page column 61, (2018/07/29)

The present invention is related to a pharmaceutical composition comprising a pharmaceutically acceptable carrier or diluent and a compound represented by the following structural formula: The present invention is also related a method of treating a subject with a disease which can be ameliorated by inhibition of poly(ADP-ribose)polymerase (PARP). The definitions of the variables are provided herein.

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