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5-羟基-1-茚酮

5-羟基-1-茚酮名称

[ CAS 号 ]:
3470-49-3

[ 中文名 ]:
5-羟基-1-茚酮

[ 英文名 ]:
5-Hydroxy-1-indanone

[中文别名 ]:

[英文别名 ]:

5-Hydroxy-2,3-dihydro-1H-inden-1-on
5-hydroxy-2,3-dihydro-1H-inden-1-one
1H-Inden-1-one, 2,3-dihydro-4-hydroxy-
4-Hydroxy-1-indanone
5-Hydroxy-1-indanone
MFCD00857527
5-hydroxy-2,3-dihydro-1H-indene-1-one
5-hydroxy-indan-1-one
4-hydroxyindan-1-one
5-hydroxy-1-oxo-2,3-dihydro-1H-indene

5-羟基-1-茚酮物理化学性质

[ 密度 ]:
1.3±0.1 g/cm3

[ 沸点 ]:
343.8±31.0 °C at 760 mmHg

[ 熔点 ]:
175 °C (dec.)(lit.)

[ 分子式 ]:
C₉H₈O₂

[ 分子量 ]:
148.159

[ 闪点 ]:
146.4±17.4 °C

[ 精确质量 ]:
148.052429

[ PSA ]:
37.30000

[ LogP ]:
1.86

[ 蒸汽压 ]:
0.0±0.8 mmHg at 25°C

[ 折射率 ]:
1.631

[ 储存条件 ]:
室温

5-羟基-1-茚酮MSDS

详细MSDS(安全技术说明书)

5-羟基-1-茚酮安全信息

[ 符号 ]:

GHS07

[ 信号词 ]:
Warning

[ 危害声明 ]:
H315-H319-H335

[ 警示性声明 ]:
P261-P305 + P351 + P338

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

[ 危害码 (欧洲) ]:
Xi:Irritant;

[ 风险声明 (欧洲) ]:
R36/37/38

[ 安全声明 (欧洲) ]:
S26-S36

[ 危险品运输编码 ]:
NONH for all modes of transport

[ WGK德国 ]:
3

[ 海关编码 ]:
2914400090

5-羟基-1-茚酮上下游产品

5-羟基-1-茚酮上游产品

5-羟基-1-茚酮下游产品

5-羟基-1-茚酮海关

[ 海关编码 ]: 2914400090

[ 中文概述 ]:
2914400090 其他酮醇及酮醛。监管条件:无。增值税率:17.0%。退税率:9.0%。最惠国关税:5.5%。普通关税:30.0%

[ 申报要素 ]: 品名, 成分含量, 用途, 丙酮报明包装

[ Summary ]:
2914400090 other ketone-alcohols and ketone-aldehydes。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:5.5%。General tariff:30.0%

5-羟基-1-茚酮文献

Synthesis and inhibition study of monoamine oxidase, indoleamine 2,3-dioxygenase and tryptophan 2,3-dioxygenase by 3,8-substituted 5H-indeno[1,2-c]pyridazin-5-one derivatives.

Eur. J. Med. Chem. 46(12) , 6104-11, (2011)

Previous studies on 5H-indeno[1,2-c]pyridazin-5-one derivatives as inhibitors of MAO-B revealed that it was possible to increase the MAO-B inhibitory potency of 5H-indeno[1,2-c]pyridazin-5-ones by sub...

On the involvement of single-bond rotation in the primary photochemistry of photoactive yellow protein. Stahl AD, et al.

Biophys. J. 101(5) , 1184-1192, (2011)

Geometric and solvent effects on intramolecular phenolic hydrogen abstraction by carbonyl n,p* and p,p* triplets. Lathioor EC and Leigh WJ.

Can. J. Chem. 79(12) , 1851-1863, (2001)

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