137775-63-4 Usage
Molecular structure
The compound has a complex molecular structure consisting of a benzene ring fused with a dioxatellurole ring and a chlorine atom attached to the benzene ring.
Ethoxyphenyl group
An ethoxyphenyl group is attached to the benzene ring, which can affect the compound's electronic properties and potential applications.
Dihydro group
The presence of a dihydro group indicates that the molecule is in a reduced state, which can influence its reactivity and stability.
Potential applications
The compound may have potential applications in various fields, including pharmaceuticals, materials science, and organic synthesis.
Further research needed
Further research is required to fully understand the properties and potential uses of this chemical compound.
Molecular weight
The molecular weight of the compound is approximately 414.95 g/mol.
Appearance
The appearance of the compound is not specified in the provided material, but it is likely a solid or a viscous liquid.
Solubility
The solubility of the compound is not specified in the provided material, but it may be soluble in organic solvents such as dichloromethane or acetone.
Check Digit Verification of cas no
The CAS Registry Mumber 137775-63-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,7,7 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 137775-63:
(8*1)+(7*3)+(6*7)+(5*7)+(4*7)+(3*5)+(2*6)+(1*3)=164
164 % 10 = 4
So 137775-63-4 is a valid CAS Registry Number.
137775-63-4Relevant academic research and scientific papers
SYNTHESIS AND STRUCTURES OF AROMATIC AND HETEROCYCLIC TELLURIUM COMPOUNDS. XXXI. REACTIONS OF ARYLTELLURIUM OXOCHLORIDES
Rivkin, B. B.,Maksimenko, A. A.,Sadekov, I. D.
, p. 1049 - 1055 (2007/10/02)
The reactions of aryltellurium oxochlorides with the lowest aliphatic acid anhydrides lead to diaryltellurium dichlorides, Te, and CO2 through the intermediate formation of diaryltellurium chloride diacylates.Aryltellurium trichlorides and carboxylic acid anhydrides are formed in the reaction with acyl chlorides.The chlorine atom in the tellurium oxochlorides is replaced by a phenyl group on reaction with phenyllithium.The reaction with dimedone in the presence of triethylamine leads to diaryl ditellurides and a product of trimerization of a carbene, viz., a dimedone derivative that is formed in the thermal decomposition of the intermediate ylid.
