所有图片(3)
About This Item
经验公式（希尔记法）:
C9H17NO5
CAS号:
分子量:
219.23
MDL编号:
UNSPSC代码:
12352209
PubChem化学物质编号:
NACRES:
NA.26
推荐产品
产品名称
Boc-Homoser-OH,
方案
>99%
表单
powder
颜色
white
应用
peptide synthesis
储存温度
−20°C
SMILES字符串
CC(C)(C)OC(=O)NC(CCO)C(O)=O
InChI
1S/C9H17NO5/c1-9(2,3)15-8(14)10-6(4-5-11)7(12)13/h6,11H,4-5H2,1-3H3,(H,10,14)(H,12,13)
InChI key
PZEMWPDUXBZKJN-UHFFFAOYSA-N
正在寻找类似产品? 访问 产品对比指南
生化/生理作用
Boc-L-homoserine is N-terminal protected α amino acid used in organic synthesis of compounds such as the functionalizable methionine surrogate azidohomoalanine.
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
A James Link et al.
Nature protocols, 2(8), 1884-1887 (2007-08-19)
This protocol describes a synthetic route to the non-canonical amino acid azidohomoalanine (AHA) using protected homoserine as a starting material. An alternative route to AHA is presented in a companion paper. This synthesis can be completed in 5 days.
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系技术服务部门