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
化学文摘社编号:
分子量:
266.34
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352112
MDL number:
产品名称
(R)-(+)-阿替洛尔, 99%
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
SMILES string
CC(C)NC[C@@H](O)COc1ccc(CC(N)=O)cc1
InChI key
METKIMKYRPQLGS-GFCCVEGCSA-N
assay
99%
optical activity
[α]25/D +16°, c = 1 in 1 M HCl
mp
148-152 °C (lit.)
functional group
amide
amine
hydroxyl
Quality Level
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存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
Joni Agustian et al.
Chirality, 29(7), 376-385 (2017-04-26)
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.
Chirality, 29(12), 847-853 (2017-10-01)
Kinetic resolution of (R,S)-atenolol is a faster strategy to produce (S)-atenolol. Since this racemate is a less soluble compound, resolution of its ester offers high concentrations in the process. A good analytical method is required to observe the enantiomer concentrations.
Kevin F Morris et al.
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Molecular dynamics simulations and NMR spectroscopy were used to compare the binding of two β-blocker drugs to the chiral molecular micelle poly-(sodium undecyl-(L)-leucine-valine). The molecular micelle is used as a chiral selector in capillary electrophoresis. This study is part of
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