方案
≥99% (HPLC)
旋光性
[α]/D -25±2°, c = 2 in ethanol
mp
127-131 °C
储存温度
2-8°C
SMILES字符串
O[C@H]([C@@H](NC(=O)[C@@H]1CCCN1)c2ccccc2)c3ccccc3
InChI
1S/C19H22N2O2/c22-18(15-10-5-2-6-11-15)17(14-8-3-1-4-9-14)21-19(23)16-12-7-13-20-16/h1-6,8-11,16-18,20,22H,7,12-13H2,(H,21,23)/t16-,17-,18-/m0/s1
InChI key
JVOUIFUIIPEWLM-BZSNNMDCSA-N
应用
(2S)-N-[(1S,2S)-2-Hydroxy-1,2-diphenylethyl]-2-pyrrolidinecarboxamide can be used as a catalyst:
- In the synthesis of α-hydroxyamino carbonyl compounds by reacting aldehydes with nitrosobenzenes via N-nitroso aldol reaction.
- In the direct aldol reactions of aldehydes with chloroacetones, methylthio- and fluoroacetones.
包装
Bottomless glass bottle. Contents are inside inserted fused cone.
警示用语:
Danger
危险声明
危险分类
Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1
储存分类代码
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
l-Proline amides catalyze direct asymmetric aldol reactions of aldehydes with methylthioacetone and fluoroacetone
Xu X, et al.
Tetrahedron Asymmetry, 18(2), 237-242 (2007)
L-Prolinamide-catalyzed direct nitroso aldol reactions of α-branched aldehydes: A distinct regioselectivity from that with L-proline
Guo H, et al.
Chemical Communications (Cambridge, England), 429-431 (2006)
L-Proline amide-catalyzed direct asymmetric aldol reaction of aldehydes with chloroacetone
He L, et al.
Tetrahedron, 62(2-3), 346-351 (2006)
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