6-Phenyl-2-pyridone

Phenylpyridone · Einecs 242-740-9 · 6-PHENYL-2-PYRIDONE · 6-phenylpyridin-2-ol · 6-Phenylpyridin-2(1H) · 6-Phenylpyridine-2-ol · 6-Phenyl-2-pyridone>6-phenyl-2-pyridone95+% · 6-Phenyl-2(1H)-pyridone

https://huagongshe.com/ko/chemical/87889

식별자 및 물리적 특성

CAS No.	19006-82-7
분자식	C11H9NO
평균 분자량	171.199 g/mol
단동위원소 질량	171.06841391 g/mol
SMILES	O=c1cccc(-c2ccccc2)[nH]1
InChIKey	ZLUIDXRFWSPPCC-UHFFFAOYSA-N
PubChem CID	87889
ChEMBL	CHEMBL1730128
EC No.	242-740-9
DTXSID	DTXSID40172472

화학 및 물리적 성질

XLogP	1.8
극성 표면적	29.1
수소 결합 공여자 수	1
수소 결합 수용자 수	1
회전 가능 결합 수	1
무거운 원자 수	13
형식 전하	0
복잡도	259
녹는점	197 °C
끓는 점	417.1±38.0 °C(Predicted)
밀도	1.158±0.06 g/cm3(Predicted)
저장 조건	Sealed in dry,2-8°C
pKa(산도 계수)	10.82±0.10(Predicted)
물리적 상태	powder to crystal
색상	White to Orange to Green
InChI	1S/C11H9NO/c13-11-8-4-7-10(12-11)9-5-2-1-3-6-9/h1-8H,(H,12,13)
InChIKey	ZLUIDXRFWSPPCC-UHFFFAOYSA-N
SMILES	O=C1NC(=CC=C1)c2ccccc2

안전 및 규제

GHS 분류	WarningH302 (97.5%): Harmful if swallowed [Warning Acute toxicity, oral]H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]P264, P264+P265, P270, P280, P301+P317, P305+P351+P338, P330, P337+P317, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 40 reports by companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.Information may vary between notifications depending on impurities, additives, and other factors. The percentage value in parenthesis indicates the notified classification ratio from companies that provide hazard codes. Only hazard codes with percentage values above 10% are shown. For more detailed information, please visit ECHA C&L website.
Hazard Classes and Categories	Acute Tox. 4 (97.5%)Eye Irrit. 2 (100%)
수질 위해 등급(WGK)	3
관세 코드	2933399990
위험 문구(R)	22-36
위험 표시	Xn
안전 문구(S)	26
위험 등급	Acute Tox. 4 OralEye Irrit. 2
저장 분류	11 - Combustible Solids

용도

6-Phenylpyridin-2(1H)-one is used as a reactant in the preparation of phenylaminopyrimidinones and its derivatives as orally active nonpeptidic inhibitors of human neutrophil elastase.