Welcome to LookChem.com Sign In|Join Free

CAS

  • or

137267-49-3

ETHYL 2-ETHYL-5-METHYLOXAZOLE-4-CARBOXYLATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

137267-49-3 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 137267-49-3 Structure

  • Basic information

    1. Product Name: ETHYL 2-ETHYL-5-METHYLOXAZOLE-4-CARBOXYLATE
    2. Synonyms: ETHYL 2-ETHYL-5-METHYLOXAZOLE-4-CARBOXYLATE
    3. CAS NO:137267-49-3
    4. Molecular Formula: C9H13NO3
    5. Molecular Weight: 183.2
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 137267-49-3.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: ETHYL 2-ETHYL-5-METHYLOXAZOLE-4-CARBOXYLATE(CAS DataBase Reference)
    10. NIST Chemistry Reference: ETHYL 2-ETHYL-5-METHYLOXAZOLE-4-CARBOXYLATE(137267-49-3)
    11. EPA Substance Registry System: ETHYL 2-ETHYL-5-METHYLOXAZOLE-4-CARBOXYLATE(137267-49-3)

  • 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: 137267-49-3(Hazardous Substances Data)

137267-49-3 Usage

Synthesis Reference(s)

Tetrahedron Letters, 35, p. 2481, 1994 DOI: 10.1016/S0040-4039(00)77149-8

Check Digit Verification of cas no

The CAS Registry Mumber 137267-49-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,2,6 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 137267-49:
(8*1)+(7*3)+(6*7)+(5*2)+(4*6)+(3*7)+(2*4)+(1*9)=143
143 % 10 = 3
So 137267-49-3 is a valid CAS Registry Number.

137267-49-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-ethyl-5-methyl-1,3-oxazole-4-carboxylate

1.2 Other means of identification

Product number -
Other names 4-OXAZOLECARBOXYLIC ACID,2-ETHYL-5-METHYL-,ETHYL 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:137267-49-3 SDS

137267-49-3Relevant articles and documents

The Oxidation of 2-Oxazolines to 1,3-Oxazoles

Meyers, A. I.,Tavares, Francis

, p. 2481 - 2484 (1994)

Oxazolines are readily oxidized to 1,3-oxazoles using NBS/peroxide or light or, more efficiently, by the Kharasch-Sosnovsky Reaction.

CpRu-catalyzed O-H insertion and condensation reactions of α-diazocarbonyl compounds

Austeri, Martina,Rix, Diane,Zeghida, Walid,Lacour, Jerome

supporting information; experimental part, p. 1394 - 1397 (2011/05/03)

[CpRu(CH3CN)3][PF6] and diimine ligands catalyze together the decomposition of α-diazocarbonyl compounds leading to O-H insertion and condensation reactions. In comparison with Rh(II) and Cu(I) complexes, the CpRu catalysts produce rapid and often more selective reactions. Promising enantioselectivities are obtained in dioxole syntheses.

Regioselectivity in the Lithiation of Methyl-substituted Thiazole- and Oxazole-Carboxylic Acids and Carboxamides: General Methods for the Elaboration of Trisubstituted Thiazoles and Oxazoles

Cornwall, Philip,Dell, Colin P.,Knight, David W.

, p. 2417 - 2428 (2007/10/02)

A number of anionic intermediates have been developed which are suitable for the elaboration of trisubstituted thiazoles and oxazoles.Thus, deprotonation of 2,4-dimethylthiazole-5-carboxylic acid 9 using either BuLi or LDA occurs regiospecifically at the

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 137267-49-3