Welcome to LookChem.com Sign In|Join Free

CAS

  • or

92234-46-3

4-Isoxazolecarboxylic acid, 4,5-dihydro-3-methyl-5-phenyl, methyl ester (9CI) is a chemical compound with the molecular formula C12H13NO3. It is a derivative of isoxazole, a heterocyclic compound containing a five-membered ring with one oxygen and one nitrogen atom. This specific compound features a methyl group at the 3-position, a phenyl group at the 5-position, and a methyl ester group at the 4-position of the isoxazole ring. It is an organic ester that can be used in various chemical reactions and synthesis processes, particularly in the pharmaceutical and agrochemical industries. The compound is known for its potential applications in the development of drugs and other bioactive molecules, due to its unique structure and reactivity.

92234-46-3 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

  • 4-Isoxazolecarboxylicacid,4,5-dihydro-3-methyl-5-phenyl-,methylester(9CI)

    Cas No: 92234-46-3

  • USD $ 1.9-2.9 / Gram

  • 100 Gram

  • 1000 Metric Ton/Month

  • Chemlyte Solutions
  • Contact Supplier
  • 92234-46-3 Structure

  • Basic information

    1. Product Name: 4-Isoxazolecarboxylicacid,4,5-dihydro-3-methyl-5-phenyl-,methylester(9CI)
    2. Synonyms: 4-Isoxazolecarboxylicacid,4,5-dihydro-3-methyl-5-phenyl-,methylester(9CI)
    3. CAS NO:92234-46-3
    4. Molecular Formula: C12H13NO3
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: ISOXAZOLE
    8. Mol File: 92234-46-3.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: 4-Isoxazolecarboxylicacid,4,5-dihydro-3-methyl-5-phenyl-,methylester(9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-Isoxazolecarboxylicacid,4,5-dihydro-3-methyl-5-phenyl-,methylester(9CI)(92234-46-3)
    11. EPA Substance Registry System: 4-Isoxazolecarboxylicacid,4,5-dihydro-3-methyl-5-phenyl-,methylester(9CI)(92234-46-3)

  • 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: 92234-46-3(Hazardous Substances Data)

92234-46-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92234-46-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,2,3 and 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 92234-46:
(7*9)+(6*2)+(5*2)+(4*3)+(3*4)+(2*4)+(1*6)=123
123 % 10 = 3
So 92234-46-3 is a valid CAS Registry Number.

92234-46-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name trans (+/-)-methyl 3-methyl-5-phenyl-2-isoxazoline-4-carboxylate

1.2 Other means of identification

Product number -
Other names (4R,5R)-3-Methyl-5-phenyl-4,5-dihydro-isoxazole-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:92234-46-3 SDS

92234-46-3Downstream Products

92234-46-3Relevant articles and documents

Synthesis of optically active 4,5-dihydroisoxazolecarboxylic acids

Zadrozna, Irmina,Kurkowska, Joanna,Makuch, Iwona

, p. 111 - 118 (2007/10/03)

A series of regioisomers of 4,5-dihydroisoxazolecarboxylates have been synthesized in the 1,3-dipolar intermolecular cycloaddition and subjected to enzymatic hydrolysis by α-chymotrypsin from bovine pancreas (type II) and to microbial hydrolysis by an Aspergillus niger fungus. For some compounds this hydrolysis time led to the obtaining of a racemic mixture, and for others the reaction was enantioselective.

4,5-Dihydroisoxazoles. Regioselectivity in the 1,3-Dipolar Cycloaddition of Nitrile Aliphatic Oxides to Cinnamic Acid esters. NMR Criteria

Zadrozna, Irmina,Kornacka, Elzbieta

, p. 363 - 372 (2007/10/03)

A systematic study of the electron and steric effects on the ratio of regioisomers of 4,5-dihydroisoxazoles has been carried out.The compounds have been prepared from aliphatic nitril oxides and methyl esters of p-substituted cinnamic acid or phenyl cinnamate.The regioisomers of substituted 4,5-dihydroisoxazoles have been established based on 1H NMR and 13C NMR spectra.

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 92234-46-3