15061-34-4 Usage
Chemical group
Imidazole group
Explanation
Different sources of media describe the Explanation of 15061-34-4 differently. You can refer to the following data:
1. 1-BENZYL-4,5-DIPHENYL-1H-IMIDAZOLE-2-THIOL belongs to the imidazole group, which is a class of organic compounds that contains a heterocyclic aromatic ring.
2. This compound contains a thiol group (-SH), making it a derivative of the imidazole ring with a sulfur-hydrogen bond.
3. A benzyl group (C6H5-CH2-) is attached to the imidazole ring, contributing to the compound's structure and properties.
4. 1-BENZYL-4,5-DIPHENYL-1H-IMIDAZOLE-2-THIOL has been studied for its potential pharmaceutical properties, including its ability to inhibit the growth of microorganisms and fungi.
5. Due to its unique chemical structure and properties, this compound may have applications in the field of material science and organic synthesis, potentially leading to the development of new materials and chemical processes.
6. The combination of the compound's chemical structure, properties, and potential applications make it a versatile option for use in multiple industries.
Thiol derivative
Yes
Benzyl group attachment
Imidazole ring
Phenyl groups
Two (4,5-positions)
Pharmaceutical properties
Antimicrobial and antifungal activities
Applications
Material science and organic synthesis
Versatility
Potential uses in various industries
Check Digit Verification of cas no
The CAS Registry Mumber 15061-34-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,0,6 and 1 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 15061-34:
(7*1)+(6*5)+(5*0)+(4*6)+(3*1)+(2*3)+(1*4)=74
74 % 10 = 4
So 15061-34-4 is a valid CAS Registry Number.
InChI:InChI=1/C22H18N2S/c25-22-23-20(18-12-6-2-7-13-18)21(19-14-8-3-9-15-19)24(22)16-17-10-4-1-5-11-17/h1-15H,16H2,(H,23,25)
15061-34-4Relevant articles and documents
Ambivalent nucleophilicity of 1,4,5-trisubstituted imidazole-2-thiones in reactions with dimethyl acetylenedicarboxylate and phenylisocyanate
Mloston,Gendek,Linden,Heimgartner
, p. 1561 - 1569 (2008/12/23)
The 1,4,5-trisubstitued 2,3-dihydro-1H-imidazole-2-thiones 1 react with electrophilic reagents via the S- or the N(3)-atom. The reaction with dimethyl acetylenedicarboxylate in methanol at room temperature occurs by the nucleophilic addition of the S-atom
RECYCLIZATION OF 4,5-DIPHENYLOXAZOLIN-2-ONE AND -2-THIONE UNDER THE INFLUENCE OF AMINES
Kalcheva, V. B.,Tsvetanska, L. I.
, p. 756 - 758 (2007/10/02)
4,5-Diphenyl-4-oxazolin-2-one and -2-thione undegro recyclization to 1-substituted 4,5-diphenyl-4-imidazolin-2-ones and -2-thiones, respectively, under the influence of primary amines.The action of hydrazine hydrate on the oxazolone leads to 5,6-diphenyl-1,2,3,4,-tetrahydro-1,2,4-triazin-3-one.The corresponding ureas were isolated from the reaction mixtures in a number of cases.
