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Assay
97%
mp
140-142 °C (lit.)
functional group
chloro
SMILES string
Cl.[O-][n+]1ccccc1Cl
InChI
1S/C5H4ClNO.ClH/c6-5-3-1-2-4-7(5)8;/h1-4H;1H
InChI key
GRZNODNSNCXOHE-UHFFFAOYSA-N
Application
2-Chloropyridine N-oxide hydrochloride was used in the synthesis of aminoheterocyclic analogs and 2-aminopyridine derivatives. It was also used in benzyl viologen enzyme assay of membrane fractions.
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
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
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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Archives of biochemistry and biophysics, 418(2), 205-216 (2003-10-03)
The ynfEFGHI operon is a paralogue of the Escherichia coli dmsABC operon. ynfE and ynfF are paralogues of dmsA. ynfG and ynfH are paralogues of dmsB and dmsC, respectively. YnfI (dmsD) has no dms paralogue. YnfE/F and YnfG could be
Bioorganic & medicinal chemistry letters, 9(13), 1801-1806 (1999-07-16)
A peptide RGD analog containing a novel 2-aminopyridine arginine mimetic was discovered to have good affinity and selectivity for the vitronectin receptor. Incorporation of the 2-aminopyridine arginine mimetic into the 3-oxo-1,4-benzodiazepine-2-acetic acid integrin antagonist series led to novel and potent
Argatroban analogs: synthesis, thrombin inhibitory activity and cell permeability of aminoheterocyclic guanidine surrogates.
Bioorganic & Medicinal Chemistry Letters, 4(18), 2165-2170 (1994)
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