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3-Isoxazolecarboxamide, 5-acetyl-4-amino- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

76390-73-3

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76390-73-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76390-73-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,3,9 and 0 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 76390-73:
(7*7)+(6*6)+(5*3)+(4*9)+(3*0)+(2*7)+(1*3)=153
153 % 10 = 3
So 76390-73-3 is a valid CAS Registry Number.

76390-73-3SDS

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 5-acetyl-4-amino-1,2-oxazole-3-carboxamide

1.2 Other means of identification

Product number -
Other names 5-ACETYL-4-AMINO-3-ISOXAZOLECARBOXAMIDE

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:76390-73-3 SDS

76390-73-3Downstream Products

76390-73-3Relevant academic research and scientific papers

Theoretical study of the mechanism of formation of 4-aminoisoxazoles. 2*. An unusual rearrangement of oximinonitriles

Kislyi,Danilova,Solkan

, p. 1042 - 1054 (2013/10/22)

The base-catalyzed cyclization of oximinonitriles in the presence of lithium ions leads to 4-aminoisoxazoles and, sometimes, to 5-aminooxazoles. Modeling using the density functional theory and the HF and MP2 methods indicated that both 4-aminoisoxazoles

4-Aminoisoxazoles by Thorpe Cyclization

Gewald, Karl,Bellmann, Peter,Jaensch, Hans-Joachim

, p. 1623 - 1629 (2007/10/02)

Cyclization of α-(acylmethoxyimino)nitriles 1 in the presence of lithium hydroxide yields 5-acyl-4-aminoisoxazoles 2.Compounds 2f and 2a can be converted into the isoxazolopyrimidone 3 and the isoxazolopyridine 4.

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