Boc-L-Valine | CAS:13734-41-3
Boc-L-Valine
- 名称：Boc-L-缬氨酸; N-叔丁氧羰基-L-缬氨酸; (S)-2-(叔丁氧基羰基-氨基)-3-甲基丁酸 | Boc-L-Valine
- CAS号：13734-41-3
- 别名：N-(tert-Butoxycarbonyl)-L-valine; N-[(1,1-Dimethylethoxy)carbonyl]-L-valine; (S)-2-(Boc-amino)-3-methylbutyric acid
- 分子式：C10H19NO4
- 分子量：217.26
- EINESC号：237-307-6
产品描述
物理化学性质
| 熔点 | 76-80 ºC |
|---|---|
| 比旋光度 | -6.3 º (c=1,CH3COOH) |
| 水溶性 | 不溶 |
安全数据
| 安全说明书 | S24/25 |
|---|
产品合成路线
文章
同行评议文献
Synthesis of trihydroxy quinolizidine alkaloids: 1, 3-addition reaction of allylmagnesium bromide to a sugar nitrone.Dhavale DD, et al. Tetrahedron, 60(13), 3009-3016 (2004)
An Efficient Asymmetric Synthesis of Tarchonanthuslactone1.Reddy M, et al. The Journal of Organic Chemistry, 66(7), 2512-2514 (2001)
Stereoselective synthesis of the antifungal antibiotic (+)-preussin.Veeresa G, et al. Tetrahedron, 54(51), 15673-15678 (1998)
Synthesis of 2-(9, 10-dihydro-9, 10-propanoanthracen-9-yl)-N-methylethanamine via a [4+ 2] cycloaddition.Karama U, et al. Molecules (Basel), 15(6), 4201-4206 (2010)
备注
Products protected by valid patents are not offered for sale in countries where the sale of such products constitutes a patent infringement and its liability is at buyer's risk.
Products currently covered by valid US Patents are offered for R&D use in accordance with 35 USC 271 +A13(1).
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