(2S)-2-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-4-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)butanoic acid(CAS: 125238-99-5)
![(2S)-2-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-4-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)butanoic acid (2S)-2-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-4-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)butanoic acid](https://cnstatic.chemtradehub.com/structs/125/125238-99-5-c6e4.webp)
CAS号
相关产品
其他供应商提供的 (2S)-2-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-4-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)butanoic acid
基本信息
分子式
C24H28N2O6
分子量
440.5 g/mol
Physical Properties
熔点
111-113°C
沸点
670.9℃ at 760 mmHg
密度
1.243
闪点
359.6℃
水溶性
Slightly soluble in water.
化学标识符
SMILES
CC(C)(C)OC(=O)NCC[C@H](NC(=O)OCC1c2ccccc2-c3ccccc13)C(=O)O
InChIKey
LIWKOFAHRLBNMG-FQEVSTJZSA-N
数据库引用
MDL号
MFCD00151941
常见问题
Fmoc-Dab(Boc)为白色固体,具有较高的结晶纯度。分子量约为454.44。在水中溶解度较低,在有机溶剂如DMF、DMSO中有较好的溶解性。该化合物具有两性反应活性,能够在酸碱条件下发生相应的化学反应。
Fmoc-Dab(Boc)通常通过Fmoc保护基团的合成来获得,首先合成Dab(Boc)酸,然后通过Fmoc保护基团的引入得到目标化合物。该合成过程通常在室温下进行,使用HOBt和DIEA作为催化剂,产率约为70%-80%。
Fmoc-Dab(Boc)主要应用于医药行业,作为合成肽类药物和蛋白质药物的中间体。此外,也可用于聚合物合成、传感器技术以及半导体材料领域。
处理Fmoc-Dab(Boc)时,应穿戴适当的个人防护装备(PPE),如实验室外套、手套和护目镜。操作应在通风橱内进行。若发生泄漏,应立即清理,并使用适当的吸收剂进行处理。处理剩余的化合物时,需遵循相关的废弃物管理规定。建议查阅最新的安全数据表(SDS)以获取更详细的安全信息。
安全须知
使用前请验证产品规格和安全数据。联系供应商获取详细安全信息。
请始终遵循正确的操作程序

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