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Merck

258903

Sigma-Aldrich

3,4-Dichloro-1,2,5-thiadiazole

97%

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About This Item

Fórmula empírica (notación de Hill):
C2Cl2N2S
Número de CAS:
Peso molecular:
155.01
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

97%

form

liquid

refractive index

n20/D 1.561 (lit.)

bp

158 °C (lit.)

density

1.648 g/mL at 25 °C (lit.)

SMILES string

Clc1nsnc1Cl

InChI

1S/C2Cl2N2S/c3-1-2(4)6-7-5-1

InChI key

YNZQOVYRCBAMEU-UHFFFAOYSA-N

Application

3,4-Dichloro-1,2,5-thiadiazole has been employed:
  • as guest molecule to investigate solid-state 13C NMR spectra of inclusion compounds of 2,6-dimethyl-bicyclo[3.3.1]nonane-exo-2-exo-6-diol with small organic molecules
  • in preparation of [1,2,5]thiadiazol-3-yl-piperazine compounds

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


Certificados de análisis (COA)

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Los clientes también vieron

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D Srinivas et al.
Rapid communications in mass spectrometry : RCM, 31(1), 121-128 (2016-10-28)
1,2,5-Thiadiazoles are an important class of compounds mostly used in synthetic chemistry, and as herbicides, insecticides, drugs, organic conductors, etc. Recently, they have been used as a source for the generation and study of nitrile N-sulfides, RCNS, and its isomers.
A L Sabb et al.
Bioorganic & medicinal chemistry letters, 11(8), 1069-1071 (2001-05-01)
Amino acid derivatives of 1,2,5-thiadiazol-3-yl-piperazine related to (+)-WAY-100135 and WAY-100635 are potent 5-HT1A receptor agonists and antagonists, which have selective affinity for 5-HT1A receptors versus alpha1 and dopamine (D2, D3, and D4) receptors.
D Gizachew et al.
Solid state nuclear magnetic resonance, 3(2), 67-78 (1994-04-01)
Solid-state 13C nuclear magnetic resonance (NMR) spectra of a number of inclusion compounds of 2,6-dimethyl-bicyclo[3.3.1]nonane-exo-2-exo-6-diol (host) with small organic small molecules (guests) have been studied. With 3,4-dichloro-1,2,5-thiadiazole and tetrachloroethylene as guests, line splittings of the host resonances were observed due

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