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Merck
CN

474835

2,4-二氟异硫氰酸苯酯

98%

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线性分子式:
F2C6H3NCS
化学文摘社编号:
141106-52-7
分子量:
171.17
UNSPSC Code:
12352100
PubChem Substance ID:
24871059
MDL number:
MFCD00041044

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InChI

1S/C7H3F2NS/c8-5-1-2-7(10-4-11)6(9)3-5/h1-3H

SMILES string

Fc1ccc(N=C=S)c(F)c1

InChI key

ABGGPKIFVAIRGU-UHFFFAOYSA-N

assay

98%

refractive index

n20/D 1.598 (lit.)

bp

46-48 °C/0.5 mmHg (lit.)

density

1.349 g/mL at 25 °C (lit.)

General description

2,4-Difluorophenyl isothiocyanate is a fluorinated building block. Its enthalpy of vaporization at boiling point (490.15K) has been reported to be 42.939kjoule/mol.

Application

2,4-Difluorophenyl isothiocyanate may be used in the synthesis of the following 2-(4-(4-X-phenylsulfonyl)benzoyl)-N-(2,4-difluorophenyl)hydrazinecarbothioamides:
  • N-(2,4-difluorophenyl)-2-(4-(phenylsulfonyl)benzoyl)hydrazinecarbothioamide
  • 2-(4-(4-chlorophenylsulfonyl)benzoyl)-N-(2,4-difluorophenyl)hydrazinecarbothioamide
  • 2-(4-(4-bromophenylsulfonyl)benzoyl)-N-(2,4-difluorophenyl)hydrazinecarbothioamide

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

10 - Combustible liquids

wgk

WGK 3

flash_point_f

199.4 °F - closed cup

flash_point_c

93 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
04196LJ
88996MJ
13328DJ
03305TH
02228ER

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Stefania-Felicia Barbuceanu et al.
International journal of molecular sciences, 15(6), 10908-10925 (2014-06-19)
In the present investigation, new hydrazinecarbothioamides 4-6 were synthesized by reaction of 4-(4-X-phenylsulfonyl)benzoic acids hydrazides (X=H, Cl, Br) 1-3 with 2,4-difluorophenyl isothiocyanate and further these were treated with sodium hydroxide to obtain 1,2,4-triazole-3-thione derivatives 7-9. The reaction of 7-9 with
Yaws CL.
Thermophysical Properties of Chemicals and Hydrocarbons, 535-535 (2014)
Fazila Rizvi et al.
Scientific reports, 9(1), 6738-6738 (2019-05-03)
A library of thiosemicarbazide derivatives of isoniazid 3-27, was synthesized and evaluated for their anti-inflammatory and urease inhibition activities, by using in vitro bioassays. Among these compounds 9, 10, 12, 21, and 26 were identified as new derivatives. Prolonged use

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