Welcome to LookChem.com Sign In | Join Free Post buying lead Chemical Tools
Home > Products > 14506-33-3

Detail of "14506-33-3"

  • CAS Number:
  • 14506-33-3
  • Name:
  • Benzenemethanol,4-chloro-a-2-propen-1-yl-

  • Molecular Structure:
  • Formula:
  • C10H11ClO
  • Molecular Weight:
  • 182.65
  • Synonyms:
  • 3-Buten-1-ol,1-(p-chlorophenyl)- (8CI);Benzenemethanol, 4-chloro-a-2-propenyl- (9CI);1-(4-Chlorophenyl)-3-buten-1-ol;1-(4-Chlorophenyl)-3-butenol;1-(p-Chlorophenyl)-3-buten-1-ol;4-(4-Chlorophenyl)but-1-en-4-ol;4-Chloro-a-2-propenylbenzenemethanol;
  • Density:
  • 1.137 g/cm3
  • Boiling Point:
  • 281.5 °C at 760 mmHg
  • Flash Point:
  • 124 °C
  • Safety:
  • 23-24/25 Details

Famous Chemical Enterprises

  • Livzon
  • Total
  • Shell
  • Dupont
  • Exxonmobil
  • Akzonobel
  • Basf
  • Bayer
  • BP
  • Business Type
  • Certificates
Please post your buying leads>>
Display:
  • Manufacturer
  • Enterprise Authentication
  • Suppiers of more reward points first
  • New supplier
Supplier of this product? Please post selling leads now!

Please post your buying leads,so that our qualified suppliers will soon contact you!
*Required Fields

Reference

Highly efficient enzymic resolution of homoallyl alcohols leading to a simple synthesis of optically pure fluoxetine and related compounds
Highly efficient enzymic resolution of homoallyl alcohols leading to a simple synthesis of optically pure fluoxetine and related compounds. Master, Hosang E.; Newadkar, R. V.; Rane, R. A.; Kumar, Ashok (St. Xavier's College, Mumbai 400 001, India). Tetrahedron Letters, 37(51), 9253-9254 (English) 1996 Elsevier. CODEN: TELEAY. ISSN: 0040-4039. DOCUMENT TYPE: Journal CA Section: 25 (Benzene, Its Derivatives, and Condensed Benzenoid Compounds) A practical method for enzymic resoln. of homoallyl alcs. and its utility in the synthesis of optically pure fluoxetine and related compds. is reported. 14506-33-3 and 77118-87-7 which are cas registry numbers of chemicals are mentioned. The enzymic resoln. of a-(2-propenyl)benzenemethanol gave (S)-a-(2-propenyl)benzenemethanol and (R)-a-(2-propenyl)benzenemethanol acetate. Ozonization and borohydride redn. of (S)-a-(2-propenyl)benzenemethanol gave (S)-1-phenyl-1,3-propanediol. The latter compd. is an intermediate for (S)-Fluoxetine hydrochloride. .
Please post your buying leads
so that our qualified suppliers will soon contact you!

©2008 LookChem.com,License:ICP NO.:Zhejiang10014259

[Hangzhou]86-571-85317600,85317603,85317620