140628-19-9 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
2. Heterocyclic compound
Explanation
A heterocyclic compound is a cyclic compound that contains atoms of at least two different elements, in this case, carbon, nitrogen, sulfur, and hydrogen.
3. Contains a triazine ring
Explanation
A triazine ring is a six-membered aromatic ring with three nitrogen atoms and three carbon atoms.
4. Contains a thione functional group
5. Used as an intermediate in the synthesis of organic compounds
Explanation
The compound serves as a starting material or building block in the production of other organic compounds, such as pharmaceuticals and agrochemicals.
6. Potential applications in the development of new materials and chemical processes
Explanation
Due to its unique structure and reactivity, the compound may be used to create new materials or improve existing chemical processes.
7. Structure and reactivity
Explanation
The specific properties and potential applications of the compound depend on its molecular structure and how it reacts with other molecules, which can be studied through experimental and computational methods.
Check Digit Verification of cas no
The CAS Registry Mumber 140628-19-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,6,2 and 8 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 140628-19:
(8*1)+(7*4)+(6*0)+(5*6)+(4*2)+(3*8)+(2*1)+(1*9)=109
109 % 10 = 9
So 140628-19-9 is a valid CAS Registry Number.
140628-19-9Relevant articles and documents
AMINOMETHYLATION OF THIOUREA DERIVATIVES WITH N-METHYLENE-tert-BUTYLAMINE. II. N,N'- AND N,N,N'-SUBSTITUTED THIOUREAS
Kovalenko, A. L.,Tselinskii, I. V.
, p. 1728 - 1730 (2007/10/02)
Reactions of 1,3-disubstituted thioureas with N-methylene-tert-butylamine without solvent proceed by a reaction of the Mannich type with formation of 1-R1-3-R2-5-tert-butyl-3,4,5,6-tetrahydro-1,3,5-triazine-2-thiones and tert-butylamine; 1,1,3-trisubstituted thioureas do not react with N-methylene-tert-butylamine as a consequence of steric hindrance, caused by the N-tert-butyl group, for the formation of the key iminium salt.
