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128406

Sigma-Aldrich

4-Fluorophenyl isothiocyanate

98%

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About This Item

Linear Formula:
FC6H4NCS
CAS Number:
1544-68-9
Molecular Weight:
153.18
Beilstein:
636596
EC Number:
216-280-4
MDL number:
MFCD00004809
UNSPSC Code:
12352100
PubChem Substance ID:
24847855
NACRES:
NA.22

Assay

98%

form

solid

bp

228 °C (lit.)

mp

24-26 °C (lit.)

storage temp.

2-8°C

SMILES string

Fc1ccc(cc1)N=C=S

InChI

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

InChI key

NFIUJHJMCQQYDL-UHFFFAOYSA-N

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Application

4-Fluorophenyl isothiocyanate has been used in the synthesis of thiourea derivatives. It has also been used in the preparation of -(4-phenylsulfonyl)-benzoic acid hydrazide.

Pictograms

Health hazardCorrosion
GHS08,GHS05

Signal Word

Danger

Hazard Statements

H314,H317,H334

Hazard Classifications

Resp. Sens. 1 - Skin Corr. 1B - Skin Sens. 1

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

192.2 °F - closed cup

Flash Point(C)

89 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

128406-BULK:
128406-5G:
128406-VAR:
128406-25G:

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Meltem Yolal et al.
Bioorganicheskaia khimiia, 38(5), 610-620 (2013-01-25)
3-Fluoro-4-(4-phenylpiperazin-1-yl)aniline (II) prepared from 3,4-difluoro nitrobenzene was converted to the corresponding Schiff bases (III) and (IV) by treatment with 4-methoxybenzaldehyde and indol-3-carbaldehyde, respectively. Treatment of amine (II) with 4-fluorophenyl isothiocyanate affordedthe corresponding thiourea derivative (V). Compound (V) was converted to
María C Soraires Santacruz et al.
Bioorganic & medicinal chemistry, 25(15), 4055-4063 (2017-06-11)
A series of N
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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