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Merck

25970

Sigma-Aldrich

3-氯苯肼 盐酸盐

≥97.0% (AT)

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About This Item

线性分子式:
ClC6H4NHNH2 · HCl
CAS号:
分子量:
179.05
Beilstein:
3565828
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:

化驗

≥97.0% (AT)

形狀

solid

mp

240-245 °C (dec.) (lit.)

SMILES 字串

Cl[H].NNc1cccc(Cl)c1

InChI

1S/C6H7ClN2.ClH/c7-5-2-1-3-6(4-5)9-8;/h1-4,9H,8H2;1H

InChI 密鑰

CRRIAWUJYMLJOE-UHFFFAOYSA-N

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應用

3-Chlorophenylhydrazine hydrochloride has been used in the preparation of:
  • 1-(3-chlorophenyl)-3,5-diphenyl-1H-pyrazolo[4,3-c]quinolin-4(5H)-one
  • 11-(3-chlorophenyl)-9-phenyl-5,6-dihydro-4H,11H-benzo[i,j]- pyrazolo[3,4-b]quinolizin-8-one
  • 1-(3-chlorophenyl)-3-(cyclohexyl)-5-(4-phenoxy phenyl)pyrazole

象形圖

Health hazardExclamation mark

訊號詞

Danger

危險聲明

危險分類

Acute Tox. 4 Oral - Resp. Sens. 1

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Ring closure reactions of 3-arylhydrazonoalkyl-quinolin-2-ones to 1-aryl-pyrazolo [4, 3-c] quinolin-2-ones.
Stadlbauer W and Hojas G.
Journal of Heterocyclic Chemistry, 41(5), 681-690 (2004)
Akihiko Tanitame et al.
Bioorganic & medicinal chemistry, 12(21), 5515-5524 (2004-10-07)
The 4-piperidyl moiety and the pyrazole ring in 1-(3-chlorophenyl)-5-(4-phenoxyphenyl)-3-(4-piperidyl)pyrazole 2, which has previously shown improved DNA gyrase inhibition and target-related antibacterial activity, were transformed to other groups and the in vitro antibacterial activity of the synthesized compounds was evaluated. The
Amina Othmani et al.
Environmental science and pollution research international, 26(25), 25969-25984 (2019-07-06)
This paper suggests a new alternative for the acceleration of dye removal by adopting alternating current instead of direct current in the treatment of methylene blue solutions and industrials effluents, using anodic oxidation on Pb/PbO2 and stainless steel (SS)/PbO2 anodes.

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