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4-Isoxazolecarboxylic acid, 5-amino-3-(2-hydroxyethoxy)-, methyl ester (9CI) is a complex organic compound with the chemical formula C7H10N2O4. It is a derivative of isoxazole, a heterocyclic compound with a five-membered ring containing one oxygen and one nitrogen atom. The molecule features an amino group (-NH2) at the 5-position, a hydroxyethoxy group (-CH2CH2OH) at the 3-position, and a methyl ester group (-COOCH3) at the 4-position. 4-Isoxazolecarboxylicacid,5-amino-3-(2-hydroxyethoxy)-,methylester(9CI) is known for its potential applications in pharmaceuticals and chemical research, particularly in the synthesis of various biologically active molecules. Its unique structure allows for a range of chemical reactions and modifications, making it a valuable intermediate in the development of new drugs and other chemical products.

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  • 4-Isoxazolecarboxylicacid,5-amino-3-(2-hydroxyethoxy)-,methylester(9CI)

    Cas No: 126865-31-4

  • USD $ 1.9-2.9 / Gram

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  • 126865-31-4 Structure
  • Basic information

    1. Product Name: 4-Isoxazolecarboxylicacid,5-amino-3-(2-hydroxyethoxy)-,methylester(9CI)
    2. Synonyms: 4-Isoxazolecarboxylicacid,5-amino-3-(2-hydroxyethoxy)-,methylester(9CI)
    3. CAS NO:126865-31-4
    4. Molecular Formula: C7H10N2O5
    5. Molecular Weight: 202.16
    6. EINECS: N/A
    7. Product Categories: AMINOACID
    8. Mol File: 126865-31-4.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,5-amino-3-(2-hydroxyethoxy)-,methylester(9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-Isoxazolecarboxylicacid,5-amino-3-(2-hydroxyethoxy)-,methylester(9CI)(126865-31-4)
    11. EPA Substance Registry System: 4-Isoxazolecarboxylicacid,5-amino-3-(2-hydroxyethoxy)-,methylester(9CI)(126865-31-4)
  • 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: 126865-31-4(Hazardous Substances Data)

126865-31-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126865-31-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,8,6 and 5 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 126865-31:
(8*1)+(7*2)+(6*6)+(5*8)+(4*6)+(3*5)+(2*3)+(1*1)=144
144 % 10 = 4
So 126865-31-4 is a valid CAS Registry Number.

126865-31-4SDS

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 5-amino-3-(2'-hydroxyethoxy)-4-methoxycarbonylisoxazole

1.2 Other means of identification

Product number -
Other names 5-Amino-3-(2-hydroxy-ethoxy)-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:126865-31-4 SDS

126865-31-4Downstream Products

126865-31-4Relevant articles and documents

Heterocyclic Compounds from 2-(Alkoxycarbonylcyanomethylene)-1,3-dioxolanes

Neidlein, Richard,Kikelj, Danijel,Kramer, Walter

, p. 1335 - 1340 (2007/10/02)

2-(Alkoxycarbonylcyanomethylene)-1,3-dioxolanes reacted with hydrazines and hydroxylamine to yield 1-substituted 4-alkoxycarbonyl-5-amino-3-(2'-hydroxyethoxy)pyrazoles and 4-alkoxycarbonyl-5-amino-3-(2'-hydroxyethoxy)isoxazoles respectively.With guanidine and benzamidine 2-substituted (R = NH2, C6H5) 5-cyano-6-(2'-hydroxyethoxy)pyrimidin-4-ones were obtained.Reaction of 2-(cyanomethoxycarbonylmethylene)-1,3-dioxolane with 1,3-diaminopropane afforded 2-(cyanomethoxycarbonylmethylene)-1,3-hexahydropyrimidine whereas treatment of the same compound with 4,5-dimethyl-1,2-phenylenediamine gave 2-(cyanomethoxycarbonylmethylene)-5,6-benzimidazoline.The structures of pyrazoles and pyrimidones were assigned on the basis of (1)H- and (13)C--nOe experiments.

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