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Merck
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Key Documents

258903

Sigma-Aldrich

3,4-二氯-1,2,5-噻二唑

97%

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About This Item

經驗公式(希爾表示法):
C2Cl2N2S
CAS號碼:
分子量::
155.01
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

品質等級

化驗

97%

形狀

liquid

折射率

n20/D 1.561 (lit.)

bp

158 °C (lit.)

密度

1.648 g/mL at 25 °C (lit.)

SMILES 字串

Clc1nsnc1Cl

InChI

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

InChI 密鑰

YNZQOVYRCBAMEU-UHFFFAOYSA-N

應用

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

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

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

標靶器官

Respiratory system

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 2

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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分析證明 (COA)

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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
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 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.

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