3-Pyridinecarboxamidine

HCID 202043CAS 23255-20-1

Basic information

Standard SMILES
N=C(N)c1cccnc1
InChIKey
FVGUUJNEJJPLCS-UHFFFAOYSA-N
Molecular formula
C6H7N3
Average molar mass
121.14 g/mol
Monoisotopic mass
121.06399724

Names & identifiers

Preferred name
3-Pyridinecarboxamidine
IUPAC
pyridine-3-carboximidamide
English name
3-Pyridinecarboxamidine
Molecular formula
C6H7N3
Molecular weight
121.14

Names & synonyms

3-Pyridinecarboxamidine23255-20-1Nicotinimidamide3-Pyridinecarboximidamidepyridine-3-carboximidamidenicotinamidinepyridine-3-carboxamidineMFCD034263233-amidinopyridinenico-tinamidineNCIOpen2_000284SCHEMBL415017
Show more names
3-PYRDINECARBOXIMIDAMIDE
3NR27EN4D8SCHEMBL2211717SCHEMBL7290798SCHEMBL31404951DTXSID40945941FVGUUJNEJJPLCS-UHFFFAOYSA-NBBL013274SBB048089

Database identifiers

CAS
23255-20-1
PubChem CID
202043
DTXSID
DTXSID40945941
UNII
3NR27EN4D8
Nikkaji
J2.140.659G

Properties

Computed structural properties

XLogP
-0.3
Topological polar surface area
62.8 Ų
Hydrogen bond donors
2
Hydrogen bond acceptors
2
Rotatable bonds
1
Heavy atoms
9

Physicochemical properties

Melting point
190 °C · 190 °C
Boiling point
241 ℃ · 241℃
Density
1.22 · 1.22
Flash point
99 ℃ · 99℃
storage temp.
2 · 2-8°C
pka
10.29 · 10.29±0.50(Predicted)

Safety & regulation

Safety data

risk_code
20/21/22-36/37/38
hazard_code
Xn
safety_code
22-26-36/37/39

Chemistry & industry

Preparation methods · 1 item

PreparationA flask containing 6.0 gm (0.058 mole) of 3-cyanopyridine dissolved in 50 ml of dry chloroform and 3.0 gm (0.065 mole) of absolute ethyl alcohol is cooled to 0°C while dry hydrogen chloride saturates the reaction mixture. The contents are allowed to stand at 0°C for 16 hr and then poured into a separatory funnel containing enough of an ice-cold 50% sodium hydroxide solution to give an alkaline solution. The mixture is shaken vigorously, then the chloroform layer is separated, washed with water until neutral, dried over potassium carbonate, and concentrated to give the crude imidate. The latter is dissolved in 20 ml of 75% aqueous ethanol containing 1.2 gm (0.0224 mole) of ammonium chloride and heated at 70°C for 4 hr, charcoal filtered, and diluted with 2 - 3 volumes of acetone. The unreacted ammonium chloride that separates is filtered, and the filtrate is again diluted with acetone until the cloud point. After standing for several hours at 0°C, 4 gm (100%), m.p. 190°C, of product separates (colorless needles).

Upstream & downstream products

Suppliers50 total

Hebei Chuanghai Biotechnology Co., Ltd+86-17732866630 · [email protected]
Career Henan Chemica Co+86-0371-86658258 +86-13203830695 · [email protected]
河南赢创生物科技有限公司16650615803 · [email protected]
苏州启航生物科技有限公司18151111370 · [email protected]
Dayang Chem (Hangzhou) Co.,Ltd.+86-0571-88938639 17705817739 · [email protected]

Related reactions

4 records

Linked notes

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