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3-氰基-6-甲基-2(1H)-吡啶酮

3-氰基-6-甲基-2(1H)-吡啶酮名称

[ CAS 号 ]:
4241-27-4

[ 中文名 ]:
3-氰基-6-甲基-2-吡啶酮

[ 英文名 ]:
Ricinidine

[中文别名 ]:

[英文别名 ]:

6-Methyl-2-oxo-1,2-dihydropyridine-3-carbonitrile
5-Cyano-6-hydroxy-2-picoline
3-Cyano-6-Methyl-2(1H)-Pyridinone
3-Cyano-6-methyl-2-pyridinol
1-Methyl-2-oxo-1,2-dihydro-3-pyridinecarbonitrile
3-Cyano-6-Methyl-2-pyridone
MFCD00006013
Ricinidine
1-Methyl-2-pyridone-3-carbonitrile
1-Methyl-2-oxo-1,2-dihydropyridine-3-carbonitrile

3-氰基-6-甲基-2(1H)-吡啶酮物理化学性质

[ 密度 ]:
1.2±0.1 g/cm3

[ 沸点 ]:
299.7±29.0 °C at 760 mmHg

[ 熔点 ]:
293-295 °C

[ 分子式 ]:
C₇H₆N₂O

[ 分子量 ]:
134.135

[ 闪点 ]:
135.0±24.3 °C

[ 精确质量 ]:
134.048019

[ PSA ]:
56.65000

[ LogP ]:
-0.54

[ 外观性状 ]:
略黄色粒状的结晶粉末

[ 蒸汽压 ]:
0.0±0.6 mmHg at 25°C

[ 折射率 ]:
1.568

[ 储存条件 ]:
室温

[ 水溶解性 ]:
2.38 g/L (20 ºC)

3-氰基-6-甲基-2(1H)-吡啶酮MSDS

3-氰基-6-甲基-2(1H)-吡啶酮安全信息

[ 符号 ]:

GHS07

[ 信号词 ]:
Warning

[ 危害声明 ]:
H302 + H312 + H332-H315-H319-H335

[ 警示性声明 ]:
P261-P280-P305 + P351 + P338

[ 个人防护装备 ]:
dust mask type N95 (US);Eyeshields;Gloves

[ 危害码 (欧洲) ]:
Xn:Harmful;

[ 风险声明 (欧洲) ]:
R20/21/22;R36/37/38

[ 安全声明 (欧洲) ]:
S36/37/39-S26-S22-S36

[ 危险品运输编码 ]:
3276

[ 包装等级 ]:
III

[ 危险类别 ]:
6.1

[ 海关编码 ]:
2933399090

3-氰基-6-甲基-2(1H)-吡啶酮合成路线

3-氰基-6-甲基-2(1H)-吡啶酮上下游产品

3-氰基-6-甲基-2(1H)-吡啶酮上游产品

3-氰基-6-甲基-2(1H)-吡啶酮下游产品

3-氰基-6-甲基-2(1H)-吡啶酮海关

[ 海关编码 ]: 2933399090

[ 中文概述 ]:
2933399090. 其他结构含非稠合吡啶环的化合物. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:20.0%

[ 申报要素 ]: 品名, 成分含量, 用途, 乌洛托品请注明外观, 6－己内酰胺请注明外观, 签约日期

[ Summary ]:
2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

3-氰基-6-甲基-2(1H)-吡啶酮文献

Synthesis, in vitro and in vivo activity of thiamine antagonist transketolase inhibitors.

Bioorg. Med. Chem. Lett. 18(6) , 2206-10, (2008)

Tumor cells extensively utilize the pentose phosphate pathway for the synthesis of ribose. Transketolase is a key enzyme in this pathway and has been suggested as a target for inhibition in the treatm...

Construction of three-dimensional supramolecular coordination copper (I) compounds with channel structures hosting a variety of anions by changing the hydrogen-bonding mode and distances. Munakata M, et al.

J. Am. Chem. Soc. 118(13) , 3117-24, (1996)

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