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HCID 202043생성일: 2026년 10월 27일

3-Pyridinecarboxamidine

Nicotinimidamide · NICOTINAMIDINE · 3-Amidinopyridine · 3-Pyridinecarboxamidine · 3-PYRDINECARBOXIMIDAMIDE · 3-Pyridinecarboximidamide

https://huagongshe.com/ko/chemical/202043

3-Pyridinecarboxamidine 분자 구조식

식별자 및 물리적 특성

CAS No.23255-20-1
분자식C6H7N3
평균 분자량121.14 g/mol
단동위원소 질량121.06399724 g/mol
SMILESN=C(N)c1cccnc1
InChIKeyFVGUUJNEJJPLCS-UHFFFAOYSA-N
PubChem CID202043
DTXSIDDTXSID40945941

화학 및 물리적 성질

XLogP-0.3
극성 표면적62.8
수소 결합 공여자 수2
수소 결합 수용자 수2
회전 가능 결합 수1
무거운 원자 수9
형식 전하0
복잡도111
녹는점190 °C
끓는 점241℃
밀도1.22
인화점99℃
저장 조건2-8°C
pKa(산도 계수)10.29±0.50(Predicted)

안전 및 규제

위험 문구(R)20/21/22-36/37/38
위험 표시Xn
안전 문구(S)22-26-36/37/39

제조 및 합성 방법

제조 방법

A 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).