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2-METHYL-1,3-BENZOXAZOLE-5-CARBOXYLIC ACID is a chemical compound characterized by its molecular formula C9H7NO3. It is a derivative of benzoxazole, a heterocyclic compound that features both nitrogen and oxygen atoms within its ring structure. The presence of a carboxylic acid group endows 2-METHYL-1,3-BENZOXAZOLE-5-CARBOXYLIC ACID with the properties of a weak organic acid, making it a versatile component in chemical processes and pharmaceutical formulations. Its unique chemical reactivity suggests potential applications in drug development and the synthesis of various organic compounds.

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  • 90322-32-0 Structure
  • Basic information

    1. Product Name: 2-METHYL-1,3-BENZOXAZOLE-5-CARBOXYLIC ACID
    2. Synonyms: 2-METHYL-1,3-BENZOXAZOLE-5-CARBOXYLIC ACID;2-METHYL-BENZOOXAZOLE-5-CARBOXYLIC ACID;OTAVA-BB 1136981;2-Methylbenzo[d]oxazole-5-carboxylic acid;2-Methyl-5-Benzoxazolecarboxylic acid;5-Benzoxazolecarboxylic acid, 2-Methyl-
    3. CAS NO:90322-32-0
    4. Molecular Formula: C9H7NO3
    5. Molecular Weight: 177.16
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 90322-32-0.mol
  • Chemical Properties

    1. Melting Point: 186-188℃
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.38
    6. Refractive Index: N/A
    7. Storage Temp.: Sealed in dry,Room Temperature
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-METHYL-1,3-BENZOXAZOLE-5-CARBOXYLIC ACID(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-METHYL-1,3-BENZOXAZOLE-5-CARBOXYLIC ACID(90322-32-0)
    11. EPA Substance Registry System: 2-METHYL-1,3-BENZOXAZOLE-5-CARBOXYLIC ACID(90322-32-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 90322-32-0(Hazardous Substances Data)

90322-32-0 Usage

Uses

Used in Pharmaceutical Formulations:
2-METHYL-1,3-BENZOXAZOLE-5-CARBOXYLIC ACID is used as an active pharmaceutical ingredient for its potential therapeutic effects. Its unique structure and reactivity may contribute to the development of new drugs with specific pharmacological properties.
Used in Chemical Processes:
In the chemical industry, 2-METHYL-1,3-BENZOXAZOLE-5-CARBOXYLIC ACID is used as a reagent or intermediate in the synthesis of various organic compounds. Its carboxylic acid group allows for a range of chemical reactions, facilitating the creation of new molecules with diverse applications.
Used in Drug Development:
2-METHYL-1,3-BENZOXAZOLE-5-CARBOXYLIC ACID is utilized as a key component in the design and synthesis of new drug candidates. Its chemical properties may offer novel mechanisms of action or improved pharmacokinetic profiles, contributing to the advancement of medicinal chemistry.
Used in Research and Development:
In academic and industrial research settings, 2-METHYL-1,3-BENZOXAZOLE-5-CARBOXYLIC ACID serves as a valuable compound for exploring new chemical reactions and understanding the underlying principles of organic chemistry. Its unique structure can provide insights into the development of innovative synthetic pathways and methodologies.

Check Digit Verification of cas no

The CAS Registry Mumber 90322-32-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,3,2 and 2 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 90322-32:
(7*9)+(6*0)+(5*3)+(4*2)+(3*2)+(2*3)+(1*2)=100
100 % 10 = 0
So 90322-32-0 is a valid CAS Registry Number.

90322-32-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Methylbenzo[d]oxazole-5-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2-Methyl-1,3-benzoxazole-5-carboxylic 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:90322-32-0 SDS

90322-32-0Relevant articles and documents

GEMINAL SUBSTITUTED QUINUCLIDINE AMIDE COMPOUNDS AS AGONISTS OF ALPHA-7 NICOTINIC ACETYLCHOLINE RECEPTORS

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Paragraph 00321-00322, (2016/07/05)

The present invention relates to novel geminal substituted quinuclidine amide compounds, and pharmaceutical compositions of the same, that are suitable as agonists or partial agonists of α7- nAChR, and methods of preparing these compounds and compositions, and the use of these compounds and compositions in methods of maintaining, treating and/or improving cognitive function. In particular, methods of administering the compound or composition to a patient in need thereof, for example a patient with a cognitive deficiency and/or a desire to enhance cognitive function, that may derive a benefit therefrom.

Novel flavors, flavor modifiers, tastants, taste enhancers, umami or sweet tastants, and/or enhancers and use thereof

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Page/Page column 40-41, (2008/06/13)

The present invention relates to the discovery that certain non-naturally occurring, non-peptide amide compounds and amide derivatives, such as oxalamides, ureas, and acrylamides, are useful flavor or taste modifiers, such as a flavoring or flavoring agents and flavor or taste enhancer, more particularly, savory (the “umami” taste of monosodium glutamate) or sweet taste modifiers,—savory or sweet flavoring agents and savory or sweet flavor enhancers, for food, beverages, and other comestible or orally administered medicinal products or compositions.

Quinuclidine-substituted hetero-bicyclic aromatic compounds for the treatment of disease

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, (2008/06/13)

The invention provides compounds of Formula I: wherein W0 is a bicyclic moiety and is These compounds may be in the form of pharmaceutical salts or compositions, may be in pure enantiomeric form or racemic mixtures, and are useful to treat diseases or conditions in which α7 is known to be involved.

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