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3-phenyl-6-methyl-7H-1,2,4-triazolo[3,4-b][1,3,4]thiadiazine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81556-04-9

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81556-04-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81556-04-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,5,5 and 6 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 81556-04:
(7*8)+(6*1)+(5*5)+(4*5)+(3*6)+(2*0)+(1*4)=129
129 % 10 = 9
So 81556-04-9 is a valid CAS Registry Number.

81556-04-9Downstream Products

81556-04-9Relevant academic research and scientific papers

Novel method for the synthesis of s -triazolo[3,4- b ][1,3,4]thiadiazines

El-Sherief, Hassan A. H.,Hozien, Zeniab A.,El-Mahdy, Ahmed F. M.,Sarhan, Abdelwareth A. O.

experimental part, p. 2636 - 2642 (2010/09/11)

The reaction of 4-amino-3-mercapto-5-phenyl-s-triazole with aromatic or aliphatic ketones containing active -hydrogens as a methyl or methylene group using an acidified acetic acid method afforded the corresponding s-triazolo[3,4-b][1,3,4]thiadiazines. In

Bicyclic Compounds Derived from 4-Amino-3-mercapto-1,2,4-triazoles: Facile Routes to 1,2,4-Triazolo[3,4-b][1,3,4]thiadiazoles and 1,2,4-Triazolo[3,4-b][1,3,4]thiadiazines

Heravi, M.M.,Rahimizadeh, M.,Seyf, M.,Davoodnia, A.,Ghassemzadeh, M.

, p. 211 - 218 (2007/10/03)

Treatment of 5-substituted-4-amino-3-mercapto-1,2,4-triazoles (1), with triethyl ortho-formate or acetyl chloride gave the corresponding triazolo[3,4-b]thiadiazoles (2) and (3), respectively. Reaction of (1) with phenacyl bromide, DMAD and DEAD afforded t

Ring Transformation of 1,3,4-Oxadiazole to s-Triazole-Fused Heterocycles. New Synthetic Route for Thiazolo-s-triazole and 7H-s-Triazolothiadiazine

Sasaki, Tadashi,Ito, Eikoh,Shimizu, Ikuo

, p. 2757 - 2760 (2007/10/02)

s-Triazole-fused heterocycles have been synthesized by an intramolecular transformation of some 1,3,4-oxadiazole ketones with ammonia or hydrazine.The α- ketone 2m gave thiazolo-s-triazole (4m), accompanied by a small amount of the hydrazide 9m on treatment with ammonium acetate in acetic acid.Similar treatment of ketones 2a and 2b afforded only the hydrazides 9a and 9b, respectively.Ketones 2a-n reacted with hydrazine hydrate in acetic acid to give 7H-s-triazolothiadiazines 5a-n.However, ketones 2o-q, with substituents α to the carbonyl group, could not be converted to the corresponding fused-ring systems.Mechanisms for these transformations are proposed.

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