88012-24-2 Usage
Description
Guanidine, N,N'-diphenyl-N''-2-thiazolyl-, a member of the guanidine family, is a white crystalline powder with a molecular formula of C17H14N4S and a molecular weight of 306.38 g/mol. It is recognized for its strong basic properties and serves as a catalyst in various chemical reactions. Guanidine, N,N'-diphenyl-N''-2-thiazolylalso exhibits potential antimicrobial and antifungal properties, making it a versatile chemical with applications across different industries.
Uses
Used in Pharmaceutical Industry:
Guanidine, N,N'-diphenyl-N''-2-thiazolylis used as an active pharmaceutical ingredient for the development of medications due to its strong basic nature and potential therapeutic effects.
Used in Agrochemical Industry:
Guanidine, N,N'-diphenyl-N''-2-thiazolylis utilized as a key component in the formulation of agrochemicals, contributing to its effectiveness in controlling pests and diseases in agriculture.
Used as a Catalyst in Chemical Reactions:
Guanidine, N,N'-diphenyl-N''-2-thiazolylis employed as a catalyst to facilitate and speed up various chemical reactions, enhancing the efficiency of industrial processes.
Used in Antimicrobial and Antifungal Applications:
Due to its potential antimicrobial and antifungal properties, Guanidine, N,N'-diphenyl-N''-2-thiazolylis used in applications requiring the control of microbial growth, such as in the development of sanitizing agents and preservatives.
Check Digit Verification of cas no
The CAS Registry Mumber 88012-24-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,0,1 and 2 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 88012-24:
(7*8)+(6*8)+(5*0)+(4*1)+(3*2)+(2*2)+(1*4)=122
122 % 10 = 2
So 88012-24-2 is a valid CAS Registry Number.
88012-24-2Relevant articles and documents
Reactions of Heteroaryliminotriphenylphosphoranes with Heterocumulenes: Synthesis and Cycloaddition Reactions of α-N-Heteroaryl-substituted Carbodiimides
Boedeker, J.,Courault, K.,Koeckritz, A.,Koeckritz, P.
, p. 463 - 474 (2007/10/02)
N-α-Heteroaryl-substituted iminotriphenylphosphoranes react with phenylisocyanate, phenylisothiocyanate, and carbon disulfide to symmetrical and unsymmetrical α-heteroarylcarbodiimides.These can not be isolated as monomeres because they behave as 1.3-diazabutadienes predominantly and form 4+2-cycloadducts.The monomeric intermediates cyclodimerize to the 1.3.5-triazines 5 resp. 14 or react by the same scheme both with phenylisocyanate and with phenylisothiocyanate to give the 1.3.5-triazines 4, resp. 12.In competition with this reaction a 2+2-cycloaddition takes place, hence there follow numerous by-products.The structure of 1.3.5- triazines is determined from hydrolysis to guanidines 6 and on the basis of spectroscopic methods.
