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100246-04-6

4-BENZOXAZOLECARBOXYLIC ACID, 2,3-DIHYDRO-2-OXO, METHYL ESTER is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 100246-04-6 Structure

  • Basic information

    1. Product Name: 4-BENZOXAZOLECARBOXYLIC ACID, 2,3-DIHYDRO-2-OXO, METHYL ESTER
    2. Synonyms: 4-BENZOXAZOLECARBOXYLIC ACID, 2,3-DIHYDRO-2-OXO, METHYL ESTER;methyl 2-oxo-2,3-dihydrobenzo[d]oxazole-4-carboxylate;2-Oxo-2,3-dihydro-benzooxazole-4-carboxylic acid methyl ester
    3. CAS NO:100246-04-6
    4. Molecular Formula: C9H7NO4
    5. Molecular Weight: 193.16
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 100246-04-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-BENZOXAZOLECARBOXYLIC ACID, 2,3-DIHYDRO-2-OXO, METHYL ESTER(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-BENZOXAZOLECARBOXYLIC ACID, 2,3-DIHYDRO-2-OXO, METHYL ESTER(100246-04-6)
    11. EPA Substance Registry System: 4-BENZOXAZOLECARBOXYLIC ACID, 2,3-DIHYDRO-2-OXO, METHYL ESTER(100246-04-6)

  • 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: 100246-04-6(Hazardous Substances Data)

100246-04-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100246-04-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,2,4 and 6 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 100246-04:
(8*1)+(7*0)+(6*0)+(5*2)+(4*4)+(3*6)+(2*0)+(1*4)=56
56 % 10 = 6
So 100246-04-6 is a valid CAS Registry Number.

100246-04-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-oxo-2,3-dihydro-benzooxazole-4-carboxylic acid methyl ester

1.2 Other means of identification

Product number -
Other names 2-Oxo-2,3-dihydro-benzooxazole-4-carboxylic acid methyl ester

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:100246-04-6 SDS

100246-04-6Relevant articles and documents

Polyheterocyclic substituted pyrimidines or pyridylamine derivatives Composition and medical application thereof

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Paragraph 0258-0259; 0261, (2021/09/26)

The invention discloses a polycyclic substituted pyrimidine or pyridine amine derivative, and the structure is shown in a formula (I). The invention further discloses a pharmaceutically acceptable salt of the derivative, a solvate, a stereoisomer, a prodrug, a pharmaceutical composition and and an application thereof in medicine. The compounds of the present invention have significant adenosine A. 2A Receptor and/or adenosine A2B The receptor antagonism activity is very practical.

2-AMINOBENZOXAZOLE CARBOXAMIDES AS 5HT3 MODULATORS

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Page/Page column 25, (2008/12/04)

Compounds of formulae I, II and III: are disclosed as 5-HT3 inhibitors. The compounds are useful in treating CINV, IBS-D and other diseases and conditions.

Rational design, synthesis, and structure-activity relationship of benzoxazolones: New potent mglu5 receptor antagonists based on the fenobam structure

Ceccarelli, Simona M.,Jaeschke, Georg,Buettelmann, Bernd,Huwyler, Joerg,Kolczewski, Sabine,Peters, Jens-Uwe,Prinssen, Eric,Porter, Richard,Spooren, Will,Vieira, Eric

, p. 1302 - 1306 (2008/09/20)

A novel class of potent and stable mGlu5 receptor antagonists was developed by combining information from a high-throughput screening campaign with the structure of the known anxiolytic fenobam. Representative compounds from this class show favorable phar

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