330884
(R)-(+)-阿替洛尔
99%
别名:
(+)-4-[2-羟基-3-[(1-甲基乙基)氨基]丙氧基]苯乙酰胺
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关于此项目
线性分子式:
(CH3)2CHNHCH2CH(OH)CH2OC6H4CH2CONH2
CAS Number:
分子量:
266.34
MDL编号:
UNSPSC代码:
12352112
PubChem化学物质编号:
NACRES:
NA.22
质量水平
方案
99%
旋光性
[α]25/D +16°, c = 1 in 1 M HCl
mp
148-152 °C (lit.)
官能团
amide
amine
hydroxyl
SMILES字符串
CC(C)NC[C@@H](O)COc1ccc(CC(N)=O)cc1
InChI
1S/C14H22N2O3/c1-10(2)16-8-12(17)9-19-13-5-3-11(4-6-13)7-14(15)18/h3-6,10,12,16-17H,7-9H2,1-2H3,(H2,15,18)/t12-/m1/s1
InChI key
METKIMKYRPQLGS-GFCCVEGCSA-N
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储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
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As the (R)-enantiomer of racemic atenolol has no β-blocking activity and no lack of side effects, switching from the racemate to the (S)-atenolol is more favorable. Transesterification of racemic atenolol using free enzymes investigated as a resource to resolve the
Joni Agustian et al.
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Chromatograms
application for HPLC我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
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