55001-04-2

Basic information

• Product Name: (+/-)-4-methyl-3-phenyl-1-pentanol
• Synonyms: (+/-)-4-methyl-3-phenyl-1-pentanol
• CAS NO: 55001-04-2
• Molecular Weight: 178.274
• Mol File: 55001-04-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: (+/-)-4-methyl-3-phenyl-1-pentanol(CAS DataBase Reference)
• NIST Chemistry Reference: (+/-)-4-methyl-3-phenyl-1-pentanol(55001-04-2)
• EPA Substance Registry System: (+/-)-4-methyl-3-phenyl-1-pentanol(55001-04-2)

Safety Data

• Hazardous Substances Data: 55001-04-2(Hazardous Substances Data)

Upstream product

• 62751-30-8 (E)-ethyl 4-methyl-3-phenylpent-2-enoate 
• 72277-17-9 (+/-)-ethyl 4-methyl-3-phenylpentanoate 
• 611-70-1 phenyl isopropyl ketone 
• 309270-99-3 (E)-4-methyl-3-phenyl-2-penten-1-ol 
• 25415-67-2 ethyl isocaproate 
• 71-43-2 benzene 
• 772-00-9 4-phenyl-1,3-dioxane 
• 75-26-3 isopropyl bromide 
• 51690-50-7 4-methyl-3-phenylpentanoic acid 
• 140-10-3 (E)-3-phenylacrylic acid 

Downstream Products

• 107202-86-8 5-methyl-4-phenylhexanenitrile 
• 55001-06-4 acid γ-isopropyl γ-phenyl butirique 
• 952755-85-0 (R)-(+)-4-methyl-3-phenyl-1-pentanol 
• 75834-20-7 (3S)-(-)-4-Methyl-3-phenyl-1-pentanol 
• 55001-05-3 [1-(2-Bromo-ethyl)-2-methyl-propyl]-benzene 

Relevant articles and documents

Enantioselective halogenative semi-pinacol rearrangement: A stereodivergent reaction on a racemic mixture

An efficient, quantitative deracemization strategy for optically inactive allylic cycloalkanols has been achieved using the biphasic halogenative semi-pinacol reaction protocol. The resultant β-halo spiroketones, containing three contiguous stereogenic ce

Lipase catalyzed acylation of primary alcohols with remotely located stereogenic centres: the resolution of (±)-4,4-dimethyl-3-phenyl-1-pentanol

Enantioselective acylation of some (±)-3-alkyl-3-phenyl-1-propanols was performed with enzymes as catalysts. Moderate enantiomeric ratios (E), ranging up to E = 11.6, were obtained. In the resolution, some of the lipases selectively acylated the (+)-enant

Generation of γ-oxy-substituted benzylithium derivatives by reductive lithiation of 4-phenyl-1,3-dioxanes

Reductive cleavage of 1,3-dioxanes 1a-c with Li metal in the presence of a catalytic amount of naphthalene in THF, followed by reaction with different electrophiles, allowed the synthesis of 3-substituted- and 3,3-disubstituted- 3-phenylpropan-1-ols 4 in good yields.