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475890

Sigma-Aldrich

2,6-Dichlorophenyl isothiocyanate

97%

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Linear Formula:
Cl2C6H3NCS
CAS Number:
6590-95-0
Molecular Weight:
204.08
MDL number:
MFCD00041056
UNSPSC Code:
12352100
PubChem Substance ID:
24871181
NACRES:
NA.22

Quality Level

100

Assay

97%

form

solid

mp

38-42 °C (lit.)

storage temp.

2-8°C

SMILES string

Clc1cccc(Cl)c1N=C=S

InChI

1S/C7H3Cl2NS/c8-5-2-1-3-6(9)7(5)10-4-11/h1-3H

InChI key

SUCGVQHNGIQXGD-UHFFFAOYSA-N

Related Categories

General description

2,6-Dichlorophenyl isothiocyanate is an isothiocyanate derivative. It has been synthesized by using 2,6-dichlorobenzaldehyde oxime as a starting reagent.

Application

2,6-Dichlorophenyl isothiocyanate may be used as a precursor to synthesize 1-(2-aminoethyl)-2-cyano-3-(2,6-dichlorophenyl)guanidine.

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Skin Corr. 1B

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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J W Tilley et al.
Journal of medicinal chemistry, 23(12), 1438-1439 (1980-12-01)
Starting with 2,6-dichlorophenyl isothiocyanate, 1-(2-aminoethyl)-2-cyano-3-(2,6-dichlorophenyl)guanidine (2) was prepared in three steps. In contrast to the corresponding thiourea 1, this compound was essentially inactive as an antihypertensive agent.
Birsa ML, et al.
Science of Synthesis: Houben-Weyl Methods of Molecular Transformations, 222-222 (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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