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Thiazolo[3,2-b][1,2,4]triazole, 6-methyl-2-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

26542-69-8

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26542-69-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26542-69-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,5,4 and 2 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 26542-69:
(7*2)+(6*6)+(5*5)+(4*4)+(3*2)+(2*6)+(1*9)=118
118 % 10 = 8
So 26542-69-8 is a valid CAS Registry Number.

26542-69-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-methyl-2-phenyl-[1,3]thiazolo[3,2-b][1,2,4]triazole

1.2 Other means of identification

Product number -
Other names 3-Methyl-6-phenyl-thiazolo(3,2-b)-1,2,4-triazole

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:26542-69-8 SDS

26542-69-8Relevant academic research and scientific papers

Unexpected direction of iodocyclization of 3-allylthio-5-phenyl-4H-1,2,4- triazole

Shmygarev,Kim

, p. 1207 - 1211 (2007/10/03)

The reaction of 3-allylthio-5-phenyl-4H-1,2,4-triazole with iodine to give a mixture of 5,6-dihydro-5-iodomethyl-3-phenyl[1,3]thiazolo[2,3-c][1,2,4] triazole, 6,7-dihydro-6-iodo-3-phenyl-5H-[1,2,4]triazolo[3,4-b][1,3]thiazine, 5,6-dihydro-6-iodomethyl-2-p

Gas-phase pyrolysis of 4-amino-3-allylthio-1,2,4-triazoles: A new route to [1,3]thiazolo[3,2-b][1,2,4]triazoles

Cartwright, Dale D.J.,Clark, Bernard A.J.,McNab, Hamish

, p. 424 - 428 (2007/10/03)

A short route to the [1,3]thiazolol[3,2-b]-[1,2,4]triazole ring system in moderate overall yield was provided by an unusual pyrolysis sequence. The carbon atoms in the fused triazole and thaizole rings were derived from a 4-aminotriazole-3-thione unit and allyl groups. Dry-flash chromatography was carried out on silica gel using a hexane-ethyl acetate gradient as eluent.

Solid acid induced heterocyclization under microwave irradiation. Highly selective synthesis of condensed thiazole

Heravi,Montazeri,Rahimizadeh,Bakavolia,Ghassemzadeh

, p. 464 - 465 (2007/10/03)

Condensed thiazoles are synthesized in satisfactory to good yields by the catalytic action of sulfuric acid adsorbed on silica gel under microwave irradiation in a solventless system.

Acid catalyzed, regioselective synthesis of 2-substituted 5- methylthiazolo[3,2-b]-S-triazoles

Heravi, Majid M.,Tajbakhsh, Mahmood,Rahimizadeh, Mohammad,Davoodnia, Abolghasem,Aghapoor, Kiumars

, p. 4417 - 4422 (2007/10/03)

The facile and regioselective synthesis of 2-substituted 5- methylthiazolo[3,2-b]triazoles has been performed by the catalytic action of H2SO4 on the corresponding propynylthio derivatives.

Sodium Hydroxide: A Mild and Inexpensive Catalyst for the Regioselective Synthesis of 2-Substituted 5-Methylthiazolo[3,2-A]-s-triazoles

Heravi, Majid M.,Tajbakhsh, Mahmood

, p. 488 - 489 (2007/10/03)

The facile and regioselective synthesis of 2-substituted 5-methylthiazolo[3,2-b]-s-triazoles has been performed by the catalytic action of NaOH on 3-propynylthio-s-triazoles.

Annelation of 3-Allenylthio-5-aryl-s-triazoles to 2-Aryl-5-methylthiazolo-s-triazoles

Upadhyaya, V. Pramod,Srinivasan, V. R.

, p. 161 - 162 (2007/10/02)

3-Propynylthio-5-aryl-s-triazoles (III) have been isomerised to 3-allenylthio-5-aryl-s-triazoles (II) in 4 percent aq. sodium hydroxide.The latter have been obtained directly by propargylation of 3-mercapto-4-aryl-s-triazoles (I) in 4 percent aq. sodium h

Sur la synthese d'acides thiazolotriazolylacetiques

Moskowitz, H.,Mignot, A.,Miocque, M.

, p. 1321 - 1323 (2007/10/02)

During the synthesis of thiazolotriazolylacetic acids, the condensation of ethyl 4-chloro-3-oxobutyrate with triazolinethiones was studied.The use of an alkaline reagent (triethylamine) leads only to S-alkylation and not to the expected cyclized product.T

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