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About This Item
Empirical Formula (Hill Notation):
C2Cl2N2S
CAS Number:
Molecular Weight:
155.01
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
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
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
10 - Combustible liquids
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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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