63649-26-3 Usage
Explanation
The compound's full name, which describes its structure and functional groups.
Explanation
The key functional groups present in the molecule that contribute to its chemical properties.
Explanation
The molecular formula represents the number of carbon (C), hydrogen (H), and oxygen (O) atoms in the compound.
Explanation
The cisconfiguration refers to the arrangement of the functional groups around the cycloalkane ring, which influences the compound's properties.
Explanation
The compound is easily soluble in organic solvents, making it suitable for various chemical reactions and applications.
Explanation
The compound is used in the production of various industrial products, as a plasticizer in polymers and resins, and as a precursor in the synthesis of pharmaceuticals and agrochemicals.
Explanation
The specific arrangement of the functional groups in the cisconfiguration gives the compound unique chemical and physical properties that make it valuable for a wide range of applications in the chemical industry.
Functional Groups
Cycloalkane, carboxylic acid, ester, and methylene
Structural Configuration
cis-
Solubility
High solubility in organic solvents
Applications
Industrial production, plasticizer, pharmaceuticals, and agrochemicals
Chemical and Physical Properties
Influenced by the cisconfiguration
Check Digit Verification of cas no
The CAS Registry Mumber 63649-26-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,6,4 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 63649-26:
(7*6)+(6*3)+(5*6)+(4*4)+(3*9)+(2*2)+(1*6)=143
143 % 10 = 3
So 63649-26-3 is a valid CAS Registry Number.
63649-26-3Relevant academic research and scientific papers
REGIOSELEKTIVE CYCLOADDITIONEN VON METHYLENCYCLOPROPAN MIT ELEKTRONENARMEN OLEFINEN AN R3P-NICKEL(O)-KATALYSATOREN.
Binger, Paul,Wedemann, Petra
, p. 1045 - 1048 (2007/10/02)
The triorganyl-phosphane/-phosphite-Ni(O) catalyzed cycloaddition of methylenecyclopropane (1) with electron deficient alkenes leads regioselectively to 2,3- or 3,4-disubstituted methylenecyclopentanes depending on the electronic properties of the ol
Reactions of Methylenecyclopropanes, V. Palladium(0)-catalyzed Codimerisation of Methylenecylopropane with Methyl Acrylates and 1,2-Ethylenedicarbonic Esters
Binger, Paul,Schuchardt, Ulf
, p. 3313 - 3324 (2007/10/02)
Triorganylphosphane-modified palladium(0) compounds catalyze the codimerisation of methylenecyclopropane (1) with methyl acrylate, methyl trans-crotonate or trans-cinnamate to give the methylenecyclopentanecarboxylic esters 3, 4, 5; diethyl fumarate or dimethyl maleate and 1 lead to the methylenecyclopentanedicarbonic esters 12.With diethyl maleate besides cis/trans-12b also oligomers containing two mols of 1 and one (cis/trans-14) or two mols of the diester (cis/trans-15) are formed.
