95898-34-3 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 5 carbon (C), 8 hydrogen (H), 2 nitrogen (N), and 2 oxygen (O) atoms.
Explanation
The compound is derived from cyclopropane, a three-carbon ring structure, with additional functional groups attached.
Explanation
The compound exists as a trans isomer, which means that the substituents on the double bond are on opposite sides of the plane formed by the carbon atoms.
Explanation
The compound has a specific stereochemistry, indicated by the (+) sign, which refers to the optical rotation of plane-polarized light. The (9CI) refers to the Chemical Abstracts Service registry number.
Explanation
The compound is used as a building block in the synthesis of more complex organic compounds and has potential applications in the development of new drugs and bioactive molecules.
Explanation
Due to its unique structural features and trans configuration, the compound can be a valuable starting material for the development of new pharmaceuticals and bioactive compounds.
Explanation
More research is needed to explore the compound's potential applications, optimize its synthesis, and determine its full range of properties and characteristics.
Structure
Cyclopropane derivative
Isomer
Trans
Stereochemistry
(+)-(9CI)
Applications
Organic synthesis and pharmaceutical research
Potential uses
Development of new drugs and bioactive molecules
Further research
Required to fully understand potential uses and properties
Check Digit Verification of cas no
The CAS Registry Mumber 95898-34-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,8,9 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 95898-34:
(7*9)+(6*5)+(5*8)+(4*9)+(3*8)+(2*3)+(1*4)=203
203 % 10 = 3
So 95898-34-3 is a valid CAS Registry Number.
95898-34-3Relevant articles and documents
THE STEREOCHEMISTRY OF THE METHYLENECYCLOPROPANE REARRANGEMENT: EVIDENCE AGAINST THE ORTHOGONAL-ALLYLIC INTERMEDIATE
Buchwalter, Stephen L.
, p. 5097 - 5112 (1984)
The rearrangements of two optically pure derivatives of Feist's acid was studied: that of dimethyl trans-methylenecyclopropane-2,3-dicarboxylate (TRANS-diester) and trans-2,3-dicyano-methylenecyclopropane (TRANS-dinitrile).The optical purity and configuration of the products, methyl(Z)- and (E)-2-carbomethoxycyclopropylideneacetate (SYN- and ANTI-diesters) and (Z)- and (E)-2-cyanocyclopropylideneacetonitrile (SYN- and ANTI-dinitriles), establish that the rearrangements occur with predominant, but not exclusive, inversion of configuration at the migrating center.Investigation of the interconversions of SYN- and ANTI- diesters and dinitriles reveal that racemic product is not obtained, as would be expected from an orthogonal-allylic diradical intermediate, but that the enantiomer corresponding to antarafacial migration is slightly favored.All of the stereochemical results are explicable by application of the Doering-Sachdev diradical transition state hypothesis.
