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1,3,4-Thiadiazole, 2-(allylamino)-5-methyl- (8CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18390-20-0

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18390-20-0 Usage

Class

Organic compounds
Belongs to the category of compounds that are primarily made of carbon and hydrogen atoms.

Subclass

Thiazoles
A subclass of organic compounds that are five-membered aromatic heterocycles containing a sulfur and a nitrogen atom.

Structural Feature

Allylamine group
The compound contains an allylamine group, which is an amine group with an allyl substituent.

Structural Feature

Methyl group
The compound has a methyl group attached to the central thiadiazole ring.

Application

Pharmaceutical industry
Used as a building block for the synthesis of various biologically active compounds, including potential drugs for the treatment of different diseases.

Application

Materials science
Has potential applications in the field of materials science due to its unique structural and chemical properties.

Application

Organic synthesis
Utilized in organic synthesis for the creation of new compounds with specific properties.

CAS Registry Number

8CI
The compound is registered under the Chemical Abstracts Service (CAS) with the identifier 8CI.

Solubility

Unknown
The solubility of the compound in various solvents is not provided in the material.

Stability

Unknown
The stability of the compound under different conditions is not provided in the material.

Reactivity

Unknown
The reactivity of the compound with other substances is not provided in the material.

Check Digit Verification of cas no

The CAS Registry Mumber 18390-20-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,3,9 and 0 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 18390-20:
(7*1)+(6*8)+(5*3)+(4*9)+(3*0)+(2*2)+(1*0)=110
110 % 10 = 0
So 18390-20-0 is a valid CAS Registry Number.

18390-20-0Downstream Products

18390-20-0Relevant academic research and scientific papers

Solvated copper(I) hexafluorosilicate π-complexes based on [Cu2(amtd)2]2+ (amtd = 2-allylamino-5-methyl-1,3,4-thiadiazole) dimer

Goreshnik,Veryasov,Morozov,Slyvka,Ardan,Mys'kiv

, p. 1 - 11 (2016)

[Cu2(amdt)2]SiF6·C6H6 and [Cu2(amdt)2(H2O)2]SiF6·CH3CN·2H2O (amdt = 2-allylamino-5-methyl-1,3,4-thiadiazole) were obtained by alternating-current electrochemical synthesis, starting from water-acetonitrile-benzene mixtures containing 2-allylamino-5-methyl-1,3,4-thiadiazole and CuSiF6·4H2O. The electrochemical reduction of the saturated copper hexafluorosilicate water solution beneath the neatly poured layer of acetonitrile-benzene amdt solution resulted in the formation of crystalline [Cu2(amdt)2]SiF6·C6H6. The initial stirring of the same mixture before subjecting it to the electrochemical reduction resulted in the formation of [Cu2(amdt)2(H2O)2]SiF6·CH3CN·2H2O. A sluggish hydrolysis of the acetonitrile over 2 years in a closed test tube with [Cu2(amdt)2]SiF6·C6H6 crystals in a mother liquor resulted in the formation of [Cu2L2(H2O)2]SiF6·CH3CONH2·2H2O. All the compounds were studied using X-ray single-crystal diffraction and Raman spectroscopy. The molecular structures and the Raman spectra of the compounds were discussed on the basis of computational modeling with the DFT/B3LYP/cc-pVDZ method.

First nγ-allyl-aminothiadiazole copper(I) φ-complexes: Synthesis and structural peculiarities of [Cu(L)CF3SO3] and [Cu 2(L)2(H2O)2](SiF6) · 2.5H2O compounds (L = 2-(allyl)-amino-5-methyl-1,3,4-thiadiazole)

Ardan, Bogdan,Slyvka, Yuriy,Goreshnik, Evgeny,Mys'kiv, Marian

, p. 484 - 490 (2013/09/23)

By means of alternating current electrochemical technique two crystalline copper(I) φ-complexes with fluorine containing anions [Cu(L)CF 3SO3] (1) and [Cu2(L)2(H 2O)2](SiF6)2 · 2.5H 2O (2) (L - 2-(allyl)-amino-5-methyl-1,3,4-thiadiazole) have been obtained and characterized by X-ray single crystal diffraction and Raman spectroscopy. In both structures the organic molecule L acts as chelate-bridging tridentate ligand being connected to copper(I) by two N atoms of thiadiazole ring and C=C bond from allyl group resulting in a formation of stable cationic dimmers SsCu(L)c2]2+. In the structure 1 oxygen atom from triflate-anion occupies an apical position of the metal coordination polyhedron, while in 2 located far from the metal centre hexafluorosilicate anion allows an appearance of the H2O molecule in copper environment. Hydrogen bonds (D)-H···A (where D = O, N, C; A = O, F) play a significant role in formation of 2D- (1) and 3D- (2) frameworks.

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