ChemicalBook Product Catalog Chemical Reagents Organic reagents Fatty alcohols 4-Phenylbutanol

4-Phenylbutanol

4-Phenylbutanol Basic information
Product Name:4-Phenylbutanol
Synonyms:4-Hexyl-1-butanol;4-PHENYL-1-BUSTANOL;1-Phenyl-4-butanol;4-PHENYL-1-BROMOBUTANE;4-PHENYL-1-BUTANOLSALMETEROL;4-Phenyl-1-butanol,97%;4-Phenyl-1-butanol 99%;4-PHENYL-1-BUTANOL
CAS:3360-41-6
MF:C10H14O
MW:150.22
EINECS:222-128-8
Product Categories:Pranlukast;Alcohols;Starting Raw Materials & Intermediates;C9 to C30;Oxygen Compounds
Mol File:3360-41-6.mol
4-Phenylbutanol Structure
4-Phenylbutanol Chemical Properties
Boiling point 140-142 °C14 mm Hg(lit.)
density 0.984 g/mL at 20 °C(lit.)
refractive index n20/D 1.521(lit.)
Fp >230 °F
storage temp. Sealed in dry,Room Temperature
solubility Chloroform
pka15.13±0.10(Predicted)
form Liquid
color Clear colorless
Odorat 100.00 %. rose
Odor Typefloral
BRN 2042122
Stability:Stable. Combustible. Incompatible with strong oxidizing agents.
InChIKeyLDZLXQFDGRCELX-UHFFFAOYSA-N
LogP2.350
CAS DataBase Reference3360-41-6(CAS DataBase Reference)
NIST Chemistry ReferenceBenzenebutanol(3360-41-6)
EPA Substance Registry SystemBenzenebutanol (3360-41-6)
Safety Information
Hazard Codes Xi,C
Risk Statements 34
Safety Statements 23-24/25-45-36/37/39-27-26
WGK Germany 3
RTECS 222-128-8
TSCA Yes
HS Code 29062900
MSDS Information
ProviderLanguage
4-Phenylbutanol English
ACROS English
SigmaAldrich English
ALFA English
4-Phenylbutanol Usage And Synthesis
Chemical Propertiescolourless liquid
Uses4-Phenyl-1-butanol is used as a reagent in the synthesis of substituted pyrrolidine-2-carboxylic acids which are used in the treatment of AT2 receptor function associated diseases.
Uses4-Phenyl-1-butanol was used in synthesis of NK105, a paclitaxel-incorporating micellar nanoparticle formulation.
Synthesis Reference(s)Chemical and Pharmaceutical Bulletin, 31, p. 2607, 1983 DOI: 10.1248/cpb.31.2607
Journal of the American Chemical Society, 73, p. 124, 1951 DOI: 10.1021/ja01145a045
General Description4-Phenyl-1-butanol is oxidized by ceric ammonium nitrate in acetonitrile to afford 2-phenyltetrahydrofuran. It undergoes cyclization in presence of phosphoric acid at high temperature to yield tetralin.
4-Phenylbutanol Preparation Products And Raw materials
Preparation ProductsPranlukast-->4-Phenylbutyryl chloride-->1-Bromo-4-phenylbutane-->BENZAL CHLORIDE-->1-CHLORO-4-PHENYLBUTANE-->BENZYL GLYCIDYL ETHER-->3-Phenyl-1-propanol-->4-Phenylbutyric acid
4-(4-Nitrophenyl)butyric acid TRANS-2-PHENYL-1-CYCLOPROPANECARBOXYLIC ACID Diphenolic acid METHYL O-METHYLPODOCARPATE 3-BENZOYLPROPIONIC ACID TIMTEC-BB SBB006499 4-(4-Methoxyphenyl)butyric acid 3-(4-Chlorobenzoyl)propionic acid CYTOCHALASIN E 4-Phenylbutanol 4-(4-METHOXYPHENYL)-1-BUTANOL CYTOCHALASIN A L-β-Homophenylalanine, HPLC 98% 4-[4-(2-CARBOXYBENZOYL)PHENYL]BUTYRIC ACID GAMMA-PHENYL-GAMMA-BUTYROLACTONE 2-PHENYLGLUTARIC ANHYDRIDE Oxytetracycline dihydrate 4,5-Dihydro-5-(4-fluorophenyl)-2(3H)-furanone
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