CAS 1083-56-3
:1,1′-(1,4-Butanediyl)bis[benzene]
Description:
1,1′-(1,4-Butanediyl)bis[benzene], also known as 1,4-bis(phenyl)butane, is an organic compound characterized by its biphenyl structure linked by a butane chain. This compound features two phenyl groups (benzene rings) connected by a four-carbon aliphatic chain, which contributes to its unique physical and chemical properties. It is typically a colorless to pale yellow solid at room temperature and is insoluble in water but soluble in organic solvents such as ethanol and ether. The presence of the butane linker provides flexibility to the molecule, influencing its conformational behavior and interactions with other substances. This compound may exhibit moderate thermal stability and can undergo typical organic reactions, including electrophilic substitution due to the electron-rich nature of the phenyl rings. Its applications may extend to materials science, particularly in the development of polymers or as intermediates in organic synthesis. Safety data should be consulted for handling, as with any chemical substance, to ensure proper precautions are taken.
Formula:C16H18
InChI:InChI=1S/C16H18/c1-3-9-15(10-4-1)13-7-8-14-16-11-5-2-6-12-16/h1-6,9-12H,7-8,13-14H2
InChI key:InChIKey=GLJFYGFBITUZOE-UHFFFAOYSA-N
SMILES:C(CCCC1=CC=CC=C1)C2=CC=CC=C2
Synonyms:- 1,1'-Butane-1,4-Diyldibenzene
- 1,1′-(1,4-Butanediyl)bis[benzene]
- 1,4-Diphenylbutene
- Benzene, 1,1'-(1,4-butanediyl)bis- (9CI)
- Benzene, 1,1′-(1,4-butanediyl)bis-
- Butane, 1,4-diphenyl-
- Butane, 1,4-diphenyl- (8CI)
- Nsc 403943
- 1,4-Diphenylbutane
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Found 5 products.
1,4-Diphenylbutane
CAS:<p>Applications 1,4-Diphenylbutane (cas# 1083-56-3) is a useful research chemical.<br></p>Formula:C16H18Color and Shape:NeatMolecular weight:210.311,4-Diphenylbutane
CAS:<p>1,4-Diphenylbutane is a modified form of the natural amino acid phenylalanine. It is used as a synthetic receptor protein for the study of the reaction between receptors and ligands. The binding of 1,4-diphenylbutane to its receptor will inhibit blood clotting by inhibiting coagulation factors. The optimal reaction occurs at pH 7.5 and at 25 degrees Celsius. The amount of 1,4-diphenylbutane required for a desired level of inhibition will depend on the type of receptor and other factors, such as temperature and concentration. The functional groups in this compound are an aromatic ring (benzene) and two alkyl chains with one carbon each (propane). This molecule has two reactive sites that can be modified by adding additional molecules to create new compounds without changing its function. In addition, 1,4-diphenylbutane binds to red blood cells more strongly than it binds</p>Formula:C16H18Purity:Min. 95%Molecular weight:210.31 g/mol





