Pentafluorophenyl N-[(9H-fluoren-9-ylmethoxy)carbonyl]-O-(2-methyl-2-propanyl)-L-tyrosinate(CAS: 86060-93-7)
![Pentafluorophenyl N-[(9H-fluoren-9-ylmethoxy)carbonyl]-O-(2-methyl-2-propanyl)-L-tyrosinate Pentafluorophenyl N-[(9H-fluoren-9-ylmethoxy)carbonyl]-O-(2-methyl-2-propanyl)-L-tyrosinate](https://cnstatic.chemtradehub.com/structs/860/86060-93-7-ef86.webp)
CAS号
相关产品
其他供应商提供的 Pentafluorophenyl N-[(9H-fluoren-9-ylmethoxy)carbonyl]-O-(2-methyl-2-propanyl)-L-tyrosinate
基本信息
分子式
C34H28F5NO5
分子量
625.59 g/mol
Physical Properties
熔点
61-64 ºC
沸点
713.3 °C at 760 mmHg
密度
1.334±0.06 g/cm3 (20 ºC 760 Torr),
闪点
713.3 °C at 760 mmHg
化学标识符
SMILES
O=C(OC1=C(F)C(F)=C(F)C(F)=C1F)[C@H](CC2=CC=C(C=C2)OC(C)(C)C)NC(OCC3C4=C(C5=C3C=CC=C5)C=CC=C4)=O
InChIKey
ADOSTZDWXCEVJP-VWLOTQADSA-N
数据库引用
MDL号
MFCD00077077
常见问题
Fmoc-O-叔-丁基-L-酪氨酸五氟苯基酯是一种有机化合物,是合成肽和蛋白质的重要保护基团之一。它由五氟苯基、叔丁基、L-酪氨酸和Fmoc侧链组成。
该化合物主要用于肽合成中的保护基反应,特别是在固相肽合成中作为氨基酸的保护基。它可以有效保护L-酪氨酸的功能基团,避免在合成过程中发生不必要的反应。
Fmoc-O-叔-丁基-L-酪氨酸五氟苯基酯相对安全,但在操作时应避免吸入粉尘或吸入其挥发性气体。在使用过程中应穿戴适当的防护装备,如手套和实验室外套。
该化合物应储存在阴凉、干燥、通风良好的地方,避免直接阳光照射。最好存放在原始包装中,以防止吸潮。储存温度应控制在室温,避免过高或过低的温度。
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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