30078-89-8

Basic information

• Product Name: α-Phenylbenzene-1-butanol
• Synonyms: α-Phenylbenzene-1-butanol;1,4-diphenylbutan-1-ol
• CAS NO: 30078-89-8
• Molecular Formula: C₁₆H₁₈O
• Molecular Weight: 226.31352
• Mol File: 30078-89-8.mol
• Article Data: 19

Chemical Properties

• Melting Point: 45-46 °C
• Boiling Point: 375.2°Cat760mmHg
• Flash Point: 155.6°C
• Appearance: /
• Density: 1.056g/cm³
• Vapor Pressure: 2.69E-06mmHg at 25°C
• Refractive Index: 1.578
• PKA: 14.32±0.20(Predicted)
• CAS DataBase Reference: α-Phenylbenzene-1-butanol(CAS DataBase Reference)
• NIST Chemistry Reference: α-Phenylbenzene-1-butanol(30078-89-8)
• EPA Substance Registry System: α-Phenylbenzene-1-butanol(30078-89-8)

Safety Data

• Hazardous Substances Data: 30078-89-8(Hazardous Substances Data)

Usage

InChI:InChI=1/C16H18O/c17-16(15-11-5-2-6-12-15)13-7-10-14-8-3-1-4-9-14/h1-6,8-9,11-12,16-17H,7,10,13H2

Upstream product

• 5407-91-0 1,4-diphenylbutan-1-one 
• 60-29-7 diethyl ether 
• 1462-75-5 3-phenylpropylmagnesium bromide 
• 100-52-7 benzaldehyde 
• 98-85-1 1-Phenylethanol 
• 60-12-8 2-phenylethanol 
• 147-93-3 Thiosalicylic acid 
• 54705-26-9 ortho-[(N-methyl)carbamoyl]phenyl benzyl sulfoxide 
• 56253-67-9 C₁₆H₁₆O 
• 15295-43-9 1-benzoyl-2-phenylcyclopropane 
• 98-86-2 acetophenone 
• 1050884-48-4 2-(4-trifluoromethyl-benzylsulfanyl)-benzoic acid 
• 20054-45-9 N-methyl-2-sulfanylbenzamide 
• 101093-83-8 2-(4-methoxy-benzylsulfanyl)-benzoic acid 

Downstream Products

• 3018-20-0 1-phenyl-1,2,3,4-tetrahydronaphthalene 
• 1142-22-9 (E)-1,4-diphenylbut-2-ene 
• 27066-35-9 (E)-1,4-diphenylbut-1-ene 
• 14213-84-4 2-phenylethylstyrene 
• 5407-91-0 1,4-diphenylbutan-1-one 

Relevant articles and documents

Chromium-Catalyzed Linear-Selective Alkylation of Aldehydes with Alkenes

We developed a chromium-catalyzed, photochemical, and linear-selective alkylation of aldehydes with alkylzirconium species generated in situ from a wide range of alkenes and Schwartz's reagent. Photochemical homolysis of the C-Zr bond afforded alkyl radicals, which were then trapped by a chromium complex catalyst to generate the alkylchromium(III) species for polar addition to aldehydes. The reaction proceeded with high functional group tolerance at ambient temperature under visible-light irradiation.

Regioselective Vinylation of Remote Unactivated C(sp3)?H Bonds: Access to Complex Fluoroalkylated Alkenes

Regioselective incorporation of a particular functional group into aliphatic sites by direct activation of unreactive C?H bonds is of great synthetic value. Despite advances in radical-mediated functionalization of C(sp3)?H bonds by a hydrogen-atom transfer process, the site-selective vinylation of remote C(sp3)?H bonds still remains underexplored. Reported herein is a new protocol for the regioselective vinylation of unactivated C(sp3)?H bonds. The remote C(sp3)?H activation is promoted by a C-centered radical instead of the commonly used N and O radicals. The reaction possesses high product diversity and synthetic efficiency, furnishing a plethora of synthetically valuable E alkenes bearing tri-/di-/mono-fluoromethyl and perfluoroalkyl groups.

Method for synthesizing alkyne through catalytic asymmetric cross coupling (by machine translation)

The invention belongs to the field of, asymmetric synthesis, and discloses a method for catalyzing asymmetric cross- coupling to synthesize: an alkyne, and the L method comprises, the following steps, of A: preparing B a cuprous, salt and C a: ligand; preparing a catalyst; adding a base; reacting the compound with the compound with the compound; and reacting the compound with the compound. Of these, one of them, X is selected from the group consisting of, R halogens. 1 Optionally substituted heteroarylsulfonylcyanamide groups selected from the, group consisting, of optionally substituted, phenyl groups In-flight vehicle, R6 Trialkyl silyl groups or alkyl radicals, R2 Cycloalkyl radicals optionally substituted with an, optionally substituted alkyl, (CH radical2 )n R4 Multi,layer chain, n＝0-10,R saw blade4 A group selected, from, the group consisting of phenyl, alkenyl, aralkynyls, noonyloxy,and, noonylsulfonylsulfonylsulfonylsulfonylsulfonylsulfonylsulfonylsulfonylsulfonylsulphonylsulphonylsulphonylsulphonylsulphonylsulphonylsulphonylsulphonylsulphonylsulphonylphenyl disiloxy-radicals. R3 A ligand, selected from hydrogen or any of the functional groups, is selected from the group consisting of, hydrogen and any L other functional group. The method, R disclosed by the, A invention has the, advantages of good catalytic, R ’ effect, wide application range. and high catalytic efficiency, and the, method disclosed by the, invention has the. advantages of good catalytic effect, wide application range and high catalytic efficiency. (by machine translation)