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Merck
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重要文件

M2209

Sigma-Aldrich

(R)-(-)-扁桃酸

98%

同義詞:

(R)-α-羟基苯乙酸

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About This Item

線性公式:
C6H5CH(OH)CO2H
CAS號碼:
分子量::
152.15
Beilstein:
2691094
EC號碼:
MDL號碼:
分類程式碼代碼:
12352106
PubChem物質ID:
NACRES:
NA.22

品質等級

化驗

98%

光學活性

[α]25/D −151°, c = 1 in ethanol

光學純度

ee: 99% (GLC)

mp

131-133 °C (lit.)

SMILES 字串

O[C@@H](C(O)=O)c1ccccc1

InChI

1S/C8H8O3/c9-7(8(10)11)6-4-2-1-3-5-6/h1-5,7,9H,(H,10,11)/t7-/m1/s1

InChI 密鑰

IWYDHOAUDWTVEP-SSDOTTSWSA-N

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象形圖

Corrosion

訊號詞

Danger

危險聲明

危險分類

Eye Dam. 1

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 1

閃點(°F)

>374.0 °F

閃點(°C)

> 190 °C

個人防護裝備

Eyeshields, Gloves, type N95 (US)


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分析證明 (COA)

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International journal of biological macromolecules, 55, 207-213 (2013-01-30)
An enantioselective S-mandelic acid (S-MA) imprinted chitosan (SMIC) was prepared by cross-linking of chitosan using formaldehyde cross-linker, in the presence of S-MA as an imprint template molecule and 0.5% acetic acid solution as a solvent. Non-imprinted cross-linked chitosan (NIC) as
Ivo B Rietveld et al.
The journal of physical chemistry. B, 115(49), 14698-14703 (2011-11-04)
In pharmacy, racemic compounds are often problematic, because generally only one of the enantiomers possesses therapeutic activity and it is often difficult to separate them. Even though this problem is likely as old as the pharmaceutical industry, one thermodynamically obvious

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