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453471

Sigma-Aldrich

4-Cyanophenylhydrazine hydrochloride

97%

Synonym(s):

4-Hydrazinobenzonitrile hydrochloride

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About This Item

Linear Formula:
NCC6H4NHNH2 · HCl
CAS Number:
2863-98-1
Molecular Weight:
169.61
MDL number:
MFCD00673994
UNSPSC Code:
12352100
PubChem Substance ID:
24868815
NACRES:
NA.22

Assay

97%

mp

241-244 °C (dec.) (lit.)

SMILES string

Cl.NNc1ccc(cc1)C#N

InChI

1S/C7H7N3.ClH/c8-5-6-1-3-7(10-9)4-2-6;/h1-4,10H,9H2;1H

InChI key

UXDLLFIRCVPPQP-UHFFFAOYSA-N

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
STBB0872V
STBB0872
S09250
10014CE
14305TD

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Małgorzata Kostecka
Molecules (Basel, Switzerland), 17(3), 3560-3573 (2012-03-24)
In view of the growing demand for new compounds showing biological activity against pathogenic microorganisms, such as pathogenic and phytopathogenic fungi, the objective of this study was to synthesize a new group of aliphatic and aromatic derivatives of hydrazide. In
Design and synthesis of new water-soluble tetrazolide derivatives of celecoxib and rofecoxib as selective cyclooxygenase-2 (COX-2) inhibitors.
Navidpour L, et al.
Bioorganic & Medicinal Chemistry Letters, 16(17), 4483-4487 (2006)
Synthesis and Structure-Activity Relationship Studies of Derivatives of the Dual Aromatase-Sulfatase Inhibitor 4-{[(4-Cyanophenyl)(4H-1,2,4-triazol-4-yl) amino] methyl} phenyl sulfamate.
Woo LW, et al.
ChemMedChem, 8(5), 779-799 (2013)

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