所有图片(1)
About This Item
线性分子式:
(CH3)3CO2CNH(CH2)7CO2H
CAS号:
分子量:
259.34
Beilstein:
2268966
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.22
方案
≥97.0%
反应适用性
reaction type: Boc solid-phase peptide synthesis
mp
56-59 °C
应用
peptide synthesis
SMILES字符串
CC(C)(C)OC(=O)NCCCCCCCC(O)=O
InChI
1S/C13H25NO4/c1-13(2,3)18-12(17)14-10-8-6-4-5-7-9-11(15)16/h4-10H2,1-3H3,(H,14,17)(H,15,16)
InChI key
FPRZYWCRQHFPSX-UHFFFAOYSA-N
其他说明
用于引入受保护的 ω-氨烷基间隔臂的试剂。更长的间隔臂通常可以提高基底的活性。
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)
其他客户在看
B J Bradbury et al.
Journal of medicinal chemistry, 33(2), 741-748 (1990-02-01)
A functionalized congener approach was used to design ligands for muscarinic cholinergic receptors (mAChRs). A series of omega-functionalized alkyl amides of N-methyl-4-(1-pyrrolidinyl)-2-butynamine (22) were prepared as functionalized analogues of UH 5 [N-methyl-N-[4-(1-pyrrolidinyl)-2-butynyl]acetamide], a muscarinic agonist related to oxotremorine. Intermediate 22
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