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1,2,4,5-Tetrazin-3(2H)-one, tetrahydro-6-methyl-2,4-bis(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87773-98-6

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87773-98-6 Usage

Family

Tetrazine derivatives

Molecular Structure

Tetrazine ring with a tetrahydro-6-methyl-2,4-bis(phenylmethyl) substituent

Potential Applications

a. Pharmaceutical industry
b. Agrochemical industry

Versatile Reactivity

Allows for various chemical reactions and modifications

Pharmacological Properties

Exhibits biological activity and potential therapeutic effects

Precursor

Can be used as a starting material in the synthesis of biologically active compounds

Unique Chemical Properties

Makes it a valuable building block for new materials and drugs

Industrial Importance

Contributes to the development of innovative products in various sectors

Check Digit Verification of cas no

The CAS Registry Mumber 87773-98-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,7,7 and 3 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 87773-98:
(7*8)+(6*7)+(5*7)+(4*7)+(3*3)+(2*9)+(1*8)=196
196 % 10 = 6
So 87773-98-6 is a valid CAS Registry Number.

87773-98-6Downstream Products

87773-98-6Relevant academic research and scientific papers

2,4-Dialkyl Substituted Carbono- and Thiocarbonohydrazides, Reactions with Carbonyl Compounds

Neugebauer, Franz Alfred,Fischer, Hans,Siegel, Rolf,Krieger, Claus

, p. 3461 - 3481 (2007/10/02)

2,4-Dialkyl substituted carbono- and thiocarbonohydrazides (4) were prepared from alkylhydrazines and phosgene or thiophosgene.Mono carbonyl compounds reacted with 4 (molar ratio 1:1) to yield hexahydro-1,2,4,5-tetrazines (9, 14; exception 13).Aldehydes in excess generally afforded dihydrazones (3); formaldehyde, however, yielded 1,1'-methylenebis(hexahydro-1,2,4,5-tetrazines) (10) as well as the bicyclic compounds 11 and 12.The constitution of 11 was confirmed by X-ray analysis of 11b.Dialdehydes and aliphatic or alicyclic α-diketones reacted with 4 to give double hexahydro-1,2,4,5-tetrazine derivatives (19), aryl substituted α-diketones on the other hand yielded cyclic dihydrazones (15) and/or mono-hexahydro-1,2,4,5-tetrazines (16).

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