14996-50-0 Usage
Description
(1,1,2,2-^2^H4)spiro[2.2]pentane is a chemical compound characterized by its unique spiro (or bridged) molecular structure, which consists of two fused rings that share a single atom. The ^2^H4 designation signifies the presence of four deuterium atoms (heavy hydrogen isotopes) within the molecule. This stable, colorless, and odorless liquid at room temperature is primarily utilized as a reactant in organic synthesis.
Uses
Used in Organic Synthesis:
(1,1,2,2-^2^H4)spiro[2.2]pentane serves as a reactant in organic synthesis, where its distinctive spiro structure and deuterium isotopes contribute to the development of novel chemical compounds and materials.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, (1,1,2,2-^2^H4)spiro[2.2]pentane is employed as a building block for the synthesis of various drug molecules. Its unique structure and deuterium content can enhance the stability, efficacy, and pharmacokinetic properties of the resulting pharmaceuticals.
Used in Agrochemical Industry:
(1,1,2,2-^2^H4)spiro[2.2]pentane is also utilized in the agrochemical industry for the synthesis of new pesticides and herbicides. Its spiro structure and deuterium isotopes can provide improved performance and selectivity for these agrochemicals.
Used in Advanced Materials:
(1,1,2,2-~2~H4)spiro[2.2]pentane (1,1,2,2-^2^H4)spiro[2.2]pentane is further employed in the development of advanced materials, such as polymers and composites, where its unique properties can lead to enhanced mechanical, thermal, or electrical characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 14996-50-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,9,9 and 6 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 14996-50:
(7*1)+(6*4)+(5*9)+(4*9)+(3*6)+(2*5)+(1*0)=140
140 % 10 = 0
So 14996-50-0 is a valid CAS Registry Number.
14996-50-0Relevant articles and documents
Laser-Powered Decomposition of Spiroalkanes (n = 2-5)
Fajgar, Radek,Pola, Josef
, p. 7709 - 7717 (2007/10/02)
The laser heating of spiroalkanes (n=2-5) and of their 1,1,2,2-tetradeuterated isotopomers reveals dissimilar modes of their thermal decomposition.Spiropentane decomposes into ethene and propadiene via two competing routes: the direct cleavage and the more important cleavage via intermediary methylenecyclobutane.Spirohexane decomposes through two important concurrent pathways which are the expulsions of ethene from the three-membered ring and a more feasible expulsion of ethene from the four-membered ring.Spiroheptane and spirooctane decompose by a radical-chain mechanism and afford complex mixtures of products; upon addition of propene both compounds rearrange into two cycloalkanes wherein the larger ring of the spiroalkane is preserved and substituted with ethylidene and a vinyl group.
