51787-79-2 Usage
Structure
Biphenyl derivative
It consists of two benzene rings connected by a central butylidene group.
Functional groups
Fluorine and iodine atoms
The compound has two fluorine atoms and one iodine atom attached to the central butylidene group.
Applications
Organic synthesis, liquid crystals, optoelectronic materials
It is used as a building block for more complex molecules in organic synthesis.
It is also used in the production of liquid crystals and optoelectronic materials.
Potential applications
Pharmaceuticals and agrochemicals
The compound may have potential uses in the development of pharmaceuticals and agrochemicals.
Hazards
Harmful if ingested or inhaled
Precautions should be taken when handling this chemical compound to avoid ingestion or inhalation.
Physical state
Likely a solid at room temperature
Based on its molecular weight and structure, it is likely that the compound is a solid at room temperature.
Solubility
Soluble in organic solvents
As a nonpolar molecule, it is expected to be soluble in organic solvents like dichloromethane, acetone, or ethanol.
Stability
Stable under normal conditions
The compound is likely stable under normal conditions, but it may be sensitive to heat, light, or moisture.
Reactivity
May react with nucleophiles and electrophiles
Due to the presence of fluorine and iodine atoms, the compound may undergo reactions with nucleophiles and electrophiles.
Check Digit Verification of cas no
The CAS Registry Mumber 51787-79-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,7,8 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 51787-79:
(7*5)+(6*1)+(5*7)+(4*8)+(3*7)+(2*7)+(1*9)=152
152 % 10 = 2
So 51787-79-2 is a valid CAS Registry Number.
51787-79-2Relevant articles and documents
Remote C(sp3)?H Arylation and Vinylation of N-Alkoxypyridinium Salts to δ-Aryl and δ-Vinyl Alcohols
Bao, Xu,Wang, Qian,Zhu, Jieping
, (2019/08/21)
The reaction of readily available and bench-stable N-alkoxypyridinium salts with arylboronic and vinylboronic acids afforded δ-aryl and δ-vinyl alcohols, respectively, in the presence of fac-Ir(ppy)3 and Cu(OTf)2 dual catalysts. The reaction takes place through a domino process involving the reductive generation of alkoxyl radicals, 1,5-hydrogen atom transfer (1,5-HAT) and the copper-catalyzed cross-coupling reaction of the resulting translocated carbon radicals with boronic acids. Complementary to the Minisci reaction, this method allows for the arylation of nucleophilic alkyl radicals with both electron-rich and electron-poor arenes under mild reaction conditions.
Modulators of the human CCR5 receptor. Part 2: SAR of substituted 1-(3,3-diphenylpropyl)-piperidinyl phenylacetamides
Cumming, John G.,Cooper, Anne E.,Grime, Ken,Logan, Chris J.,McLaughlin, Sharon,Oldfield, John,Shaw, John S.,Tucker, Howard,Winter, Jon,Whittaker, David
, p. 5012 - 5015 (2007/10/03)
SAR and DMPK studies led to the identification of substituted N-alkyl-N-[1-(3,3-diphenylpropyl)piperidin-4-yl]-2-phenylacetamides as potent and orally bioavailable ligands for the human CCR5 chemokine receptor.
