Welcome to LookChem.com Sign In|Join Free
  • or
1-(3-fluorophenyl)-pentan-1-ol is an organic compound with the molecular formula C11H15FO. It is a colorless liquid at room temperature and has a molecular weight of 180.23 g/mol. 1-(3-fluorophenyl)-pentan-1-ol is characterized by the presence of a fluorophenyl group (a phenyl ring with a fluorine atom) attached to a pentanol chain (a five-carbon alcohol chain). The fluorine atom in the 3-position of the phenyl ring imparts unique electronic and steric properties to the molecule, which can affect its reactivity and physical properties. 1-(3-fluorophenyl)-pentan-1-ol is used in the synthesis of various pharmaceuticals and agrochemicals due to its potential to modulate biological activity. It is also a valuable intermediate in the preparation of more complex organic molecules.

1598-19-2

Post Buying Request

1598-19-2 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

1598-19-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1598-19-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,9 and 8 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1598-19:
(6*1)+(5*5)+(4*9)+(3*8)+(2*1)+(1*9)=102
102 % 10 = 2
So 1598-19-2 is a valid CAS Registry Number.

1598-19-2Relevant academic research and scientific papers

Direct transformation of aryl 2-pyridyl esters to secondary benzylic alcohols by nickel relay catalysis

Wu, Xianqing,Li, Xiaobin,Huang, Wenyi,Wang, Yun,Xu, Hui,Cai, Liangzhen,Qu, Jingping,Chen, Yifeng

supporting information, p. 2453 - 2458 (2019/03/29)

A direct transformation of aryl esters to secondary benzylic alcohols via tandem Ni-catalyzed cross-coupling reactions of aromatic 2-pyridyl esters with alkyl zinc reagents and carbonyl group reduction by Ni-H species is achieved. Preliminary mechanistic studies reveal that the Ni-H species is generated in situ via β-hydride elimination of the Negishi reagents. The reaction is catalyzed by bench-stable nickel salts under mild conditions with wide functional group tolerance.

Synthesis and mesomorphic properties of laterally fluorinated alkyl 4′′-alkylterphenyl-4-yl carbonate liquid crystals

Choluj, Artur,Kula, Przemyslaw,Dabrowski, Roman,Tykarska, Marzena,Jaroszewicz, Leszek

, p. 891 - 900 (2014/01/23)

Fifteen series of homologues of a variety of mono-, di- and trifluorosubstituted alkyl 4′′-alkylterphenyl-4-yl carbonates have been synthesized and their mesomorphic properties have been determined. From among 95 prepared compounds, 40 pure nematogens have been found, as well as 55 mesogens with orthogonal and tilted smectic phases in broad temperature ranges. The type and combination of the LC phase strongly depend on the position and number of the fluorine atoms. Physical properties and correlations between the molecular core fluorosubstitution, the length of the terminal chains and the type and sequence of the liquid crystalline phases, have been determined. The compounds are useful for the formulation of nematic mixtures as well as ferroelectric ones.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 1598-19-2