250598-32-4 Usage
Cyclic organosilicon compound
The compound has a silacyclohexane ring, which is a six-membered ring containing silicon and carbon atoms.
Silacyclohexane ring
The ring structure consists of alternating silicon and carbon atoms, with two oxygen atoms attached to the silicon atom.
Two oxygen atoms attached to the silicon atom
The presence of oxygen atoms in the ring contributes to the compound's unique chemical properties.
Two methyl groups
The compound has two methyl groups (CH3) attached to the cyclic ring, which are small alkyl groups.
Isopropyl group
The compound also contains an isopropyl group (C3H7) attached to the cyclic ring, which is a larger alkyl group.
Reactant in organic synthesis
The compound is primarily used as a starting material in the synthesis of various silicon-containing compounds.
Applications in pharmaceuticals, agrochemicals, and materials science
Due to its unique chemical structure and properties, the compound has potential uses in these fields for the development of new products and materials.
9CI
The term "9CI" refers to the Chemical Abstracts Service registry number, which is a unique identifier for this specific compound.
Check Digit Verification of cas no
The CAS Registry Mumber 250598-32-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,0,5,9 and 8 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 250598-32:
(8*2)+(7*5)+(6*0)+(5*5)+(4*9)+(3*8)+(2*3)+(1*2)=144
144 % 10 = 4
So 250598-32-4 is a valid CAS Registry Number.
250598-32-4Relevant articles and documents
Configuration and predominant conformations of 5-isopropyl-2,2,4-trimethyl-1,3-dioxa-2-silacyclohexane stereoisomers
Kuznetsov,Gvozdik,Bochkor,Novikov,Spirikhin
, p. 778 - 783 (2007/10/03)
The stereochemistry of 5-isopropyl-2,2,4-trimethyl-1,3-dioxa-2-silacyclohexane (mixture of stereoisomers) and model 5-isopropyl-2,2-dimethyl-1,3-dioxa-2-silacyclohexane was studied by 1H and 13C NMR spectroscopy. The molecules of the latter compound and of the trans isomer of the trimethyl derivative exist mainly in the chair conformation with the equatorial isopropyl group, and the molecules of the cis isomer, in the 3,6-twist form. The experimental data were confirmed by AM1 and MM2 calculations of the optimal geometry.
