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等級
for chiral derivatization
品質等級
化驗
≥99.0% (sum of enantiomers, GC)
≥99.0%
形狀
liquid
光學活性
[α]20/D −10.5±0.5°, neat
光學純度
enantiomeric ratio: ≥99.5:0.5 (GC)
品質
LiChropur™
技術
HPLC: suitable
折射率
n20/D 1.513
n20/D 1.5145 (lit.)
bp
55-56 °C/2.5 mmHg (lit.)
密度
1.045 g/mL at 20 °C (lit.)
儲存溫度
2-8°C
SMILES 字串
C[C@H](N=C=O)c1ccccc1
InChI
1S/C9H9NO/c1-8(10-7-11)9-5-3-2-4-6-9/h2-6,8H,1H3/t8-/m0/s1
InChI 密鑰
JJSCUXAFAJEQGB-QMMMGPOBSA-N
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訊號詞
Danger
危險分類
Acute Tox. 2 Inhalation - Aquatic Chronic 3 - Eye Irrit. 2 - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
6.1A - Combustible, acute toxic Cat. 1 and 2 / very toxic hazardous materials
水污染物質分類(WGK)
WGK 3
閃點(°F)
149.0 °F - closed cup
閃點(°C)
65 °C - closed cup
個人防護裝備
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Journal of enzyme inhibition and medicinal chemistry, 17(6), 375-379 (2003-04-10)
The derivatization of racemic 5-[(2-methylphenoxy)methyl]-2-amino-2-oxazoline, developed as an imidazoline binding sites ligand, with (+)-(R)-alpha-methylbenzyl isocyanate was performed in chloroform. The reaction led to two pairs of diastereomers, which were separated by RP-HPLC. A kinetic study of the derivatization reaction was
High-performance liquid chromatographic determination of the enantiomers of beta-adrenoceptor blocking agents in biological fluids. II. Studies with atenolol.
Journal of chromatography, 489(2), 438-445 (1989-04-14)
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