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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
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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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.
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.
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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