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387825-03-8

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387825-03-8 Usage

General Description

Salclobuzic acid, also known as salicylhydroxamic acid, is a chemical compound with the formula C8H7NO3. It is derived from salicylic acid and has been synthesized for its potential use as an antineoplastic and antituberculosis agent. Salclobuzic acid functions as a chelating agent, meaning it can bind to metal ions, and it has been studied for its ability to inhibit the growth of tumor cells. Additionally, it has been investigated for its potential to boost the efficacy of certain antibiotics in treating tuberculosis. However, further research is needed to fully understand the potential pharmacological properties and toxicity of salclobuzic acid before it can be applied in clinical settings.

Check Digit Verification of cas no

The CAS Registry Mumber 387825-03-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,7,8,2 and 5 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 387825-03:
(8*3)+(7*8)+(6*7)+(5*8)+(4*2)+(3*5)+(2*0)+(1*3)=188
188 % 10 = 8
So 387825-03-8 is a valid CAS Registry Number.

387825-03-8SDS

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 4-[(4-chloro-2-hydroxybenzoyl)amino]butanoic acid

1.2 Other means of identification

Product number -
Other names 4-[(2-hydroxy-4-chlorobenzoyl)amino]butanoate

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:387825-03-8 SDS

387825-03-8Downstream Products

387825-03-8Relevant articles and documents

4-CNAB and preparation method thereof

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Paragraph 0038; 0042-0043; 0050; 0053; 0055; 0058, (2020/11/26)

The invention discloses 4-CNAB and a preparation method thereof, and belongs to the field of drug preparation. According to the technical scheme, the preparation method comprises the following steps:S1, adding dichloromethane into 4-chlorosalicylic acid, adding sodium bentonite and N, N-carbonyl diimidazole, then adding ethyl 4-aminobutyrate hydrochloride, dropwise adding triethylamine, adding adiluted hydrochloric acid solution, adjusting the pH value to 4.5-5, performing suction filtration, collecting filtrate, sequentially extracting with dilute ammonia water, pure water and a saturated sodium chloride solution, and concentrating an organic phase to obtain an intermediate I; S2, dissolving the intermediate I with a sodium hydroxide solution, dropwise adding a dilute hydrochloric acidsolution, adjusting the pH value to 4.5-5, separating out a product, and carrying out suction filtration and drying to obtain free acid; S3, dissolving free acid with isopropanol, adding a sodium hydroxide solution, after a reaction is carried out for 1 h, supplementing isopropanol and reacting for 1-2 h, performing suction filtration and drying to obtain 4-CNAB. The yield of each step is high, the product purity is good, and the salified product is easy for suction filtration.

Compounds and compositions for delivering active agents

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, (2008/06/13)

Compounds and compositions for the delivery of active agents are provided. Methods of administration and preparation are provide as well.

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