210230-86-7 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 9 carbon (C), 16 hydrogen (H), 2 nitrogen (N), and 1 oxygen (O) atoms.
Explanation
The molecular weight is the mass of one mole of a substance, measured in grams per mole (g/mol). For this compound, the molecular weight is 168.24 g/mol.
3. Heterocyclic organic compound
Explanation
A heterocyclic organic compound is a cyclic compound containing atoms of at least two different elements, in this case, carbon, nitrogen, and oxygen.
4. Diazocinone family derivative
Explanation
The compound belongs to the diazocinone family, which is a group of chemical compounds characterized by a specific ring structure containing nitrogen and oxygen atoms.
Explanation
Synonyms are alternative names for a chemical compound. In this case, the compound is also known as tetrahydro-8-isopropyl-3,4,6,7-tetrahydro-1,4-diazocine-5-one.
6. Chemical synthesis and research applications
Explanation
The compound is used in chemical synthesis and research, although specific applications and properties are not well-documented.
Molecular weight
168.24 g/mol
Synonyms
Tetrahydro-8-isopropyl-3,4,6,7-tetrahydro-1,4-diazocine-5-one
Structure
Six-membered ring with nitrogen and oxygen atoms, and a tetrahydro-8-isopropyl group
Check Digit Verification of cas no
The CAS Registry Mumber 210230-86-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,0,2,3 and 0 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 210230-86:
(8*2)+(7*1)+(6*0)+(5*2)+(4*3)+(3*0)+(2*8)+(1*6)=67
67 % 10 = 7
So 210230-86-7 is a valid CAS Registry Number.
210230-86-7Relevant articles and documents
An efficient approach to γ-alkylidene γ-butyrolactones: Application to the syntheses of pyridazinones and diazocinones
Reddy, Ravinder S.,Saravanan,Kumar, Pradeep
, p. 6553 - 6564 (2007/10/03)
The efficient phototransformation of a variety of spirodiones 3 to γ- alkylidene γ butyrolactones 4 and their application to the syntheses of biologically useful pyridazinones 14 and diazocinones 15 are described.
