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Merck
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文件

330884

Sigma-Aldrich

(R)-(+)-阿替洛尔

99%

同義詞:

(+)-4-[2-羟基-3-[(1-甲基乙基)氨基]丙氧基]苯乙酰胺

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About This Item

線性公式:
(CH3)2CHNHCH2CH(OH)CH2OC6H4CH2CONH2
CAS號碼:
56715-13-0
分子量：:
266.34
MDL號碼:
MFCD00074917
分類程式碼代碼:
12352112
PubChem物質ID:
24859921
NACRES:
NA.22

化驗

99%

光學活性

[α]25/D +16°, c = 1 in 1 M HCl

mp

148-152 °C (lit.)

SMILES 字串

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 密鑰

METKIMKYRPQLGS-GFCCVEGCSA-N

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儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)

分析證明 (COA)

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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.
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
Kevin F Morris et al.
Chemical physics, 457, 133-146 (2015-08-11)
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
Ulisse Garbin et al.
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The endothelium plays a key role in the development of atherogenesis and its inflammatory and proliferative status influences the progression of atherosclerosis. The aim of this study is to compare the effects of two beta blockers such as nebivolol and

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