(<I>S</I>)-3-叠氮基-2-(Fmoc-氨基)丙酸

产品名称：

684270-46-0
Fmoc-β-azido-Ala-OH
(S)-3-Azido-2-(Fmoc-amino)propionic acid
Fmoc-3-azido-L-alanine
Fmoc-β-叠氮-Ala-OH
Fmoc-3-叠氮基-L-丙氨酸
(S)-3-叠氮基-2-(Fmoc-氨基)丙酸

产品介绍：

产品说明

应用

Fmoc-β-azido-Ala-OH chloride is a general N-terminal protected reagent used in the solid phase peptide synthesis. Azido group allows it to undergo copper-mediated click chemistry reactions.
It can be used in:

Synthesis of α-N-acetylgalactosamine (α-GalNAc) linked antifreeze glycopeptides (AFGPs).
Synthesis of stimuli-responsive multifunctional peptide gatekeepers for drug delivery applications.
Synthesis of triazole-linked glycopeptides via Cu(I)-catalyzed 1,3-dipolar cycloaddition (CuAAC).

包装

250 mg in glass bottle
Bottomless glass bottle. Contents are inside inserted fused cone.

基本信息

经验(实验)分子式	C₁₈H₁₆N₄O₄
分子量	352.34
MDL编号	MFCD11052919
PubChem化学物质编号	329763258
NACRES	NA.26

产品性质

质量水平	100
测定	≥98.0% (HPLC)
旋光性	[α]/D -10.0±1.0°, c = 1 in DMF
reaction suitability	reaction type: Fmoc solid-phase peptide synthesis reaction type: click chemistry
杂质	15.3-16.5% nitrogen 60.1-62.5% carbon
application(s)	peptide synthesis
官能团	Fmoc
储存温度	2-8℃
SMILES string	OC(=O)[C@H](CN=[N+]=[N-])NC(=O)OCC1c2ccccc2-c3ccccc13
InChI	1S/C18H16N4O4/c19-22-20-9-16(17(23)24)21-18(25)26-10-15-13-7-3-1-5-11(13)12-6-2-4-8-14(12)15/h1-8,15-16H,9-10H2,(H,21,25)(H,23,24)/t16-/m0/s1
InChI key	ZITYCUDVCWLHPG-INIZCTEOSA-N

安全信息

储存分类代码	13 - Non Combustible Solids
WGK	WGK 3
闪点(F)	Not applicable
闪点(C)	Not applicable
个人防护装备	dust mask type N95 (US), Eyeshields, Gloves