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2-FLUOROPHENYL ISOTHIOCYANATE

  • Name 2-FLUOROPHENYL ISOTHIOCYANATE
  • CAS 38985-64-7
  • Purity 99%
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Product Details

Bulk supply high purity 2-FLUOROPHENYL ISOTHIOCYANATE 38985-64-7, Paid sample available

  • Molecular Formula: C7H4FNS
  • Molecular Weight: 153.18
  • Appearance/Colour: colorless to light yellow liquid 
  • Vapor Pressure: 0.129mmHg at 25°C 
  • Melting Point: 24-26 °C 
  • Refractive Index: 1.6254 
  • Boiling Point: 225.4 °C at 760 mmHg 
  • Flash Point: 97.2 °C 
  • PSA: 44.45000 
  • Density: 1.15 g/cm3 
  • LogP: 2.56000 

2-FLUOROPHENYL ISOTHIOCYANATE(Cas 38985-64-7) Usage

InChI:InChI=1/C7H4FNS/c8-6-3-1-2-4-7(6)9-5-10/h1-4H

38985-64-7 Relevant articles

Design, synthesis and biological evaluation of novel 2,4-disubstituted quinazoline derivatives targeting H1975 cells via EGFR-PI3K signaling pathway

Chao, Gao,Dai, Honglin,Ke, Yu,Li, Erdong,Lihong, Shan,Liu, Hongmin,Liu, Limin,Si, Xiaojie,Wang, Zhengjie,Yang, Zhang,Zhang, Luye,Zhang, Qiurong,Zheng, Jiaxin

, (2021/07/28)

In order to find new and highly effectiv...

Triton-B catalyzed one pot multicomponent synthesis of isothiocyanates in non-aqueous medium

Singh, Neha,Khare, Richa

, p. 1636 - 1638 (2019/06/11)

A facile and novel method to synthesize ...

A with nematode-killing activity containing N, S heterocyclic compound and its preparation and use

-

, (2019/02/19)

The present invention relates to a compo...

Direct, Microwave-Assisted Synthesis of Isothiocyanates

Janczewski, ?ukasz,Gajda, Anna,Gajda, Tadeusz

, p. 2528 - 2532 (2019/04/03)

A microwave-assisted desulfuration of re...

38985-64-7 Process route

carbon disulfide
75-15-0,12122-00-8

carbon disulfide

2-Fluoroaniline
348-54-9

2-Fluoroaniline

o-fluorophenyl isothiocyanate
38985-64-7

o-fluorophenyl isothiocyanate

Conditions
Conditions Yield
carbon disulfide; 2-Fluoroaniline; In dimethyl sulfoxide; for 0.25h; Inert atmosphere;
With N-benzyl-trimethylammonium hydroxide; In dimethyl sulfoxide; for 2h; Inert atmosphere;
97%
carbon disulfide; 2-Fluoroaniline; In acetone; at 20 ℃;
With iron(II) sulfate; triethylamine; In acetone; chemoselective reaction;
80%
With ammonia; In ethanol;
carbon disulfide; 2-Fluoroaniline; With sodium hydroxide; Heating;
With chloroformic acid ethyl ester; Heating;
carbon disulfide; 2-Fluoroaniline; In methanol;
With BCT; In chloroform;
carbon disulfide; 2-Fluoroaniline; With triethylamine; In toluene; at 20 ℃; for 9h;
In dichloromethane; for 3h; Reflux;
carbon disulfide; 2-Fluoroaniline; With 1,4-diaza-bicyclo[2.2.2]octane; In acetone; at 20 ℃;
With bis(trichloromethyl) carbonate; In chloroform; at 0 - 20 ℃;
2-Fluoroaniline
348-54-9

2-Fluoroaniline

thiophosgene
463-71-8

thiophosgene

o-fluorophenyl isothiocyanate
38985-64-7

o-fluorophenyl isothiocyanate

Conditions
Conditions Yield
With triethylamine; In toluene;
76%
With triethylamine; In dichloromethane; at 20 ℃; for 1h;
With sodium hydrogencarbonate; In chloroform; water; at 0 - 20 ℃; for 6h;

38985-64-7 Upstream products

  • 75-15-0
    75-15-0

    carbon disulfide

  • 348-54-9
    348-54-9

    2-Fluoroaniline

  • 463-71-8
    463-71-8

    thiophosgene

  • 51085-49-5
    51085-49-5

    2-fluoroaniline hydrochloride

38985-64-7 Downstream products

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    N-(2-fluorophenyl)-2-methylpropanethioamide

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