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Thiazolo[4,5-d]isoxazol-5-amine, 3-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

193346-77-9

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193346-77-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 193346-77-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,3,3,4 and 6 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 193346-77:
(8*1)+(7*9)+(6*3)+(5*3)+(4*4)+(3*6)+(2*7)+(1*7)=159
159 % 10 = 9
So 193346-77-9 is a valid CAS Registry Number.

193346-77-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-amino-3-phenyl-thiazolo[4,5-d]isoxazole

1.2 Other means of identification

Product number -
Other names 5-amino-3-phenylthiazolo[4,5-d]isoxazole

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:193346-77-9 SDS

193346-77-9Downstream Products

193346-77-9Relevant academic research and scientific papers

New synthetic methods: Part I - Regioselective 1, 2-transposition of carbonyl group in carbocyclic and heterocyclic ketones

Chande, Madhukar S.,Amle, Anand P.

, p. 2625 - 2627 (2007/10/03)

A convenient and simple synthetic method for 1, 2- transposition of keto group in pyrazol-5-ones, indan-1,3-dione and benzofuran-3-one is described.

On the synthesis of fused thiazolo[5,4-d]isoxazoles and a novel rearrangement involving conversion of 5(4H)-isoxazolones to 4(5H)-isoxazolones

Chande,Joshi

, p. 403 - 409 (2007/10/03)

The interaction of 4-bromo-3-substituted-(4H)-isoxazol-5-ones (1) with alkyl/aryl thiocarbamides (2), 4-alkyl/aryl thiosemicarbazides (7) and 2, 4-disubstituted thiosemicarbazides (12) afford 5-alkyl/ arylamino-3-substituted-thiazolo [5, 4-d]isoxazoles (3) and 6-amino/anilino-5-alkyl/arylimino-3-substituted-thiazolo[5, 4-d]isoxazoles respectively. An alternate unambiguous one step synthesis is described. The compounds have been characterised by chemical reactions and spectral data.

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