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化工社化工社 化学情報印刷レポート · 研究参考用
HCID 87889作成日:2026年10月27日

6-フェニル-2-ピリドン

6-フェニル-2-ピリドン · 6-フェニル-2(1H)-ピリドン · 6-フェニルピリジン-2-オール · 6-フェニル-2(1H)-ピリジノン · >95% · 6-フェニル-2-ピリジノール · 6-フェニルピリジン-2(1H)-オン · 6-フェニル-1,2-ジヒドロピリジン-2-オン

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

6-フェニル-2-ピリドン の分子構造式

識別子と物理属性

CAS No.19006-82-7
分子式C11H9NO
平均分子量171.199 g/mol
単同位体質量171.06841391 g/mol
SMILESO=c1cccc(-c2ccccc2)[nH]1
InChIKeyZLUIDXRFWSPPCC-UHFFFAOYSA-N
PubChem CID87889
ChEMBLCHEMBL1730128
EC No.242-740-9
DTXSIDDTXSID40172472
現地名6-フェニル-2-ピリドン

化学・物理的性質

XLogP1.8
極性表面積29.1
水素結合供与体数1
水素結合受容体数1
回転可能結合数1
重原子数13
形式電荷0
複雑度259
融点197 °C
沸点417.1±38.0 °C(Predicted)
密度1.158±0.06 g/cm3(Predicted)
貯蔵条件Sealed in dry,2-8°C
pKa(酸解離定数)10.82±0.10(Predicted)
外観・状態powder to crystal
色White to Orange to Green
InChI1S/C11H9NO/c13-11-8-4-7-10(12-11)9-5-2-1-3-6-9/h1-8H,(H,12,13)
InChIKeyZLUIDXRFWSPPCC-UHFFFAOYSA-N
SMILESO=C1NC(=CC=C1)c2ccccc2
CAS データベース19006-82-7

安全性と法規制

GHS 分類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 CategoriesAcute Tox. 4 (97.5%)Eye Irrit. 2 (100%)
水環境危害等級(WGK)3
税関コード2933399990
危険文句(R)22-36
危険表示Xn
安全措置(S)26
危険等級Acute Tox. 4 OralEye Irrit. 2
貯蔵分類11 - Combustible Solids

用途

使用

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.