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51-01-4

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51-01-4 Usage

Description

2,4-bis(acetyloxy)benzoic acid, commonly known as aspirin, is a versatile chemical compound that belongs to the class of nonsteroidal anti-inflammatory drugs (NSAIDs). It is widely recognized for its ability to relieve pain, reduce fever, and decrease inflammation by inhibiting the production of certain chemicals in the body. Aspirin also has potential cardiovascular and anti-cancer benefits, making it an important medication with a broad range of therapeutic effects.

Uses

Used in Pain Relief and Fever Reduction:
Aspirin is used as an analgesic and antipyretic agent for the management of mild to moderate pain and fever. It works by inhibiting the production of prostaglandins, which are chemicals responsible for pain, fever, and inflammation.
Used in Cardiovascular Health:
Aspirin is used as an antiplatelet agent to prevent heart attacks and strokes in individuals at high risk. It inhibits platelet aggregation, reducing the risk of blood clot formation and improving blood flow.
Used in Anti-cancer Applications:
Aspirin has been found to possess potential anti-cancer properties, although the exact mechanisms are still under investigation. It may help reduce the risk of certain types of cancer, such as colorectal cancer, by modulating various cellular pathways and processes.
Used in Pharmaceutical Industry:
Aspirin is used as an active pharmaceutical ingredient in various formulations, such as tablets, capsules, and suppositories, for the treatment of pain, fever, inflammation, and cardiovascular conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 51-01-4 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 5 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 51-01:
(4*5)+(3*1)+(2*0)+(1*1)=24
24 % 10 = 4
So 51-01-4 is a valid CAS Registry Number.

51-01-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-diacetyloxybenzoic acid

1.2 Other means of identification

Product number -
Other names 2,4-diacetoxybenzoic 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:51-01-4 SDS

51-01-4Relevant articles and documents

Improved compsn. antiallergic habitus

-

, (2007/10/06)

PROBLEM TO BE SOLVED: To provide a composition for ameliorating allergic constitution naturally ingestible in daily life. SOLUTION: The composition for ameliorating the allergic constitution comprises a galactooligosaccharide as a main ingredient. Furthermore, a food and drink uses the composition. Since the galactooligosaccharide is already widely used in heath-oriented foods such as a specific food for health and is a material in which the safety is sufficiently established, the galactooligosaccharide is naturally ingestible over a long period in the daily life. COPYRIGHT: (C)2007,JPOandINPIT

Synergistically acting compositions for selectively combating tumor tissue

-

, (2008/06/13)

According to the invention, compositions are made available which have a strong cytotoxic effect which is largely selective on tumor tissue. The invention is based on the fact that certain benzoic acid derivatives have a strong synergistic effect as a mixture and destroy cancer cells selectively in a pH range of 7 or below, such as from 6.5 to 7.

Cobalt(II)-Catalyzed Reaction of Aldehydes with Acetic Anhydride under an Oxygen Atmosphere: Scope and Mechanism

Bhatia, Beena,Punniyamurthy, T.,Iqbal, Javed

, p. 5518 - 5523 (2007/10/02)

The reaction of aldehydes with acetic anhydride in the presence of catalytic cobalt(II) chloride under an oxygen atmosphere at ambient temperature is dependent upon the reaction medium.Aliphatic aldehydes react in acetonitrile to give 1,2-diones whereas the aromatic aldehydes are acylated to yield the corresponding acylals.On the other hand, carboxylic acids are obtained from aliphatic and aromatic aldehydes by conducting the reaction in dichloroethane or benzene.Cobalt(II) chloride in acetonitrile catalyzes the conversion of aliphatic aldehydes to the correspondinganhydrides in the absence of acetic anhydride whereas aromatic aldehydes remain largely unaffected under these conditions.A preliminary mechanistic study in three different solvents (i.e. acetonitrile, dichloroethane, and DMF) has revealed that in acetonitrile and in the presence of acetic anhydride, aliphatic aldehydes behave differently than aromatic aldehydes.Some trapping experiments using methyl acrylate and stilbene have been conducted to demonstrate the occurence of an acyl cobalt and peroxyacyl cobalt intermediate during these reactions.

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