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5-Bromo-N,2-dihydroxybenzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

5798-94-7

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5798-94-7 Usage

Purification Methods

Crystallise the hydroxamic acid from H2O (m 249o) or from EtOH (m 232o dec). It sublimes at m 235o. It complexes with metals. [Beilstein 10 IV 221.]

Check Digit Verification of cas no

The CAS Registry Mumber 5798-94-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,9 and 8 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5798-94:
(6*5)+(5*7)+(4*9)+(3*8)+(2*9)+(1*4)=147
147 % 10 = 7
So 5798-94-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H6BrNO3/c8-4-1-2-6(10)5(3-4)7(11)9-12/h1-3,10,12H,(H,9,11)

5798-94-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name sodium,4-bromo-2-(hydroxycarbamoyl)phenolate

1.2 Other means of identification

Product number -
Other names 5-bromo-2-hydroxy-benzohydroxamic acid

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:5798-94-7 SDS

5798-94-7Relevant academic research and scientific papers

FUSED HETEROCYCLIC COMPOUNDS AS ION CHANNEL MODULATORS

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Paragraph 0468; 0469, (2015/07/02)

The present disclosure relates to compounds that are sodium channel inhibitors and to their use in the treatment of various disease states, including cardiovascular diseases and diabetes. In particular embodiments, the structure of the compounds is given

Synthesis and biological evaluation of D-amino acid oxidase inhibitors

Ferraris, Dana,Duvall, Bridget,Ko, Yao-Sen,Thomas, Ajit G.,Rojas, Camilo,Majer, Pavel,Hashimoto, Kenji,Tsukamoto, Takashi

supporting information; experimental part, p. 3357 - 3359 (2009/04/07)

D-Amino acid oxidase (DAAO) catalyzes the oxidation of D-amino acids including D-serine, a full agonist at the glycine site of the NMDA receptor. A series of benzo[d]isoxazol-3-ol derivatives were synthesized and evaluated as DAAO inhibitors. Among them,

Mixed anhydrides of carbamic and hydroxamic acids

-

, (2008/06/13)

A base precursor represented by the following general formula (A) or (B): STR1 wherein A1, A2, A5, A6, A7, and A8 each represents a hydrogen atom, an alkyl group, a substituted alkyl group, a cycloalkyl group, an alkenyl group, an aralkyl group, an aryl group, a substituted aryl group, an acyl group, or a heterocyclic group, and A1 and A2 can combine to form a ring and two of A5, A6, A7, and A8 can combine to form a ring, A3 and A4 each represents a hydrogen atom, an alkyl group, a substituted alkyl group, a cycloalkyl group, or an aralkyl group, and A3 and A4 can combine to form a ring or A3 and A4 can be a double bond forming an imino group from STR2 and X represents a nucleophilic group.

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