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65422-70-0

Methyl 2-oxo-2,3-dihydro-1,3-benzoxazole-5-carboxylate is a chemical compound characterized by the molecular formula C10H9NO4. It is a stable and versatile intermediate widely used in the synthesis of pharmaceuticals and agrochemicals. Methyl 2-oxo-2,3-dihydro-1,3-benzoxazole-5-carboxylate is recognized for its diverse applications across medicine, agriculture, and material science, serving as a valuable building block for the production of biologically active compounds and contributing to the development of new drugs and pesticides.

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  • 65422-70-0 Structure

  • Basic information

    1. Product Name: Methyl 2-oxo-2,3-dihydro-1,3-benzoxazole-5-carboxylate
    2. Synonyms: Methyl 2-oxo-2,3-dihydro-1,3-benzoxazole-5-carboxylate;methyl 2-oxo-2,3-dihydrobenzo[d]oxazole-5-carboxylate
    3. CAS NO:65422-70-0
    4. Molecular Formula: C9H7NO4
    5. Molecular Weight: 193.157
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 65422-70-0.mol

  • Chemical Properties

    1. Melting Point: 194-196°
    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: Methyl 2-oxo-2,3-dihydro-1,3-benzoxazole-5-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: Methyl 2-oxo-2,3-dihydro-1,3-benzoxazole-5-carboxylate(65422-70-0)
    11. EPA Substance Registry System: Methyl 2-oxo-2,3-dihydro-1,3-benzoxazole-5-carboxylate(65422-70-0)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 65422-70-0(Hazardous Substances Data)

65422-70-0 Usage

Uses

Used in Pharmaceutical Industry:
Methyl 2-oxo-2,3-dihydro-1,3-benzoxazole-5-carboxylate is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to undergo multiple chemical reactions, leading to the production of a broad spectrum of biologically active compounds.
Used in Agrochemical Industry:
In the agrochemical sector, Methyl 2-oxo-2,3-dihydro-1,3-benzoxazole-5-carboxylate is utilized as a precursor in the development of new pesticides, leveraging its chemical reactivity to create effective and novel agrochemical products.
Used in Material Science:
Methyl 2-oxo-2,3-dihydro-1,3-benzoxazole-5-carboxylate is employed in material science applications due to its potential to form derivatives that can enhance or impart specific properties to materials, contributing to advancements in various material technologies.

Check Digit Verification of cas no

The CAS Registry Mumber 65422-70-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,4,2 and 2 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 65422-70:
(7*6)+(6*5)+(5*4)+(4*2)+(3*2)+(2*7)+(1*0)=120
120 % 10 = 0
So 65422-70-0 is a valid CAS Registry Number.

65422-70-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-oxo-3H-1,3-benzoxazole-5-carboxylate

1.2 Other means of identification

Product number -
Other names methyl 2-oxo-2,3-dihydrobenzoxazole-5-carboxylate

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:65422-70-0 SDS

65422-70-0Relevant articles and documents

INHIBITORS OF ENL/AF9 YEATS

-

Paragraph 00104-00106, (2021/06/26)

Methods and compositions for treating leukemia are disclosed. Acylated 6-aminoindoles, acylated 6-aminopyrrolopyridines and acylated 3-aminopyrrolo[3,2-c]pyridazines of the following formula inhibit ENL/AF9 YEATS and are therefore useful for treating leukemia.

Synthetic approaches to amino analogues of N-acetylcolchinol

Colombel, Virginie,Baudoin, Olivier

supporting information; experimental part, p. 4329 - 4335 (2009/09/25)

(Chemical Equation Presented) A straightforward synthesis of aminodibenzoxepines, new analogues of N-acetylcolchinol, is reported by using two different strategies. The first strategy involves a Grignard addition, a biaryl Suzuki-Miyaura coupling, and a H

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