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3-Amidinopyridine hydrochloride, 97%|140457|7356-60-7

3-Amidinopyridine hydrochloride, 97%

Cat. No JK140457_5_G
J&K Chemical

Product Information

Product Name
3-Amidinopyridine hydrochloride, 97%
Brand Name
J&K
Product Number
140457
CAS
7356-60-7
Molecular Formula
C6H7N3·HCl
Molecular Weight
157.60
SDS Document
View/Download
Certificate of Analysis (COA)​
COA not found

General Information

Synonyms
3-Amidinopyridinium chloride
PubChem CID
202042
IUPAC Name
pyridine-3-carboximidamide;hydrochloride
InChI Key
MKJPBOVLAZADQJ-UHFFFAOYSA-N
SMILES
C1=CC(=CN=C1)C(=N)N.Cl

Properties

Melting Point
187-189

Safety Information

Signal Word
Warning
Hazard Statement
H302
H312
H316
H320
H332
H335
Precautionary Statement
P270
P330
P501
P280
P321
P261
P271
P319
P405
P301+P317
P302+P352
P362+P364
P332+P317
P264+P265
P305+P351+P338
P337+P317
P304+P340
P403+P233

References Data Source From Pubchem

Synthesis of 2-arylquinazolines by Chan–Evans–Lam coupling of 2-formylphenylboronic acids with amidines
Publication Name: Chemistry of Heterocyclic Compounds
Publication Date: 2024-04
DOI: 10.1007/s10593-024-03314-2

Reaction of 3-Alkoxycyclobutanones with Amidines
Publication Name: Science of Synthesis
Publication Date: 2020

Synthesis of Novel Five- and Six-Membered Ferrocene-Containing Heterocycles and Heteroaromatics via Cyclocondensation of 1-Ferro­cenyl-3,3-bis(methylthio)prop-2-en-1-one with Various Bifunctional Nucleophiles
Publication Name: Synthesis
Publication Date: 2017-03-10
DOI: 10.1055/s-0036-1588966

Reaction of Dibenz[b,f]oxepin-10(11H)-one with Base and Carbon Disulfide/Iodomethane or Dimethyl Trithiocarbonate; Annulation of the Products
Publication Name: Science of Synthesis
Publication Date: 2012

Recyclization reactions of 2-(1-benzoylpyrrolidin- 2-ylidene)malononitrile
Publication Name: Chemistry of Heterocyclic Compounds
Publication Date: 2010-04-30
DOI: 10.1007/s10593-010-0469-2

3-Amidinopyridine hydrochloride, 97%

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