N-{trans-4-[4-(Cyclopropylmethyl)-1-piperazinyl]cyclohexyl}-4-{[(7R)-7-ethyl-8-isopropyl-5-methyl-6-oxo-5,6,7,8-tetrahydro-2-pteridinyl]amino}-3-methoxybenzamide(CAS: 755038-65-4)
![N-{trans-4-[4-(Cyclopropylmethyl)-1-piperazinyl]cyclohexyl}-4-{[(7R)-7-ethyl-8-isopropyl-5-methyl-6-oxo-5,6,7,8-tetrahydro-2-pteridinyl]amino}-3-methoxybenzamide N-{trans-4-[4-(Cyclopropylmethyl)-1-piperazinyl]cyclohexyl}-4-{[(7R)-7-ethyl-8-isopropyl-5-methyl-6-oxo-5,6,7,8-tetrahydro-2-pteridinyl]amino}-3-methoxybenzamide](https://cnstatic.chemtradehub.com/structs/755/755038-65-4-5c08.webp)
CAS号
相关产品
其他供应商提供的 N-{trans-4-[4-(Cyclopropylmethyl)-1-piperazinyl]cyclohexyl}-4-{[(7R)-7-ethyl-8-isopropyl-5-methyl-6-oxo-5,6,7,8-tetrahydro-2-pteridinyl]amino}-3-methoxybenzamide
基本信息
分子式
C34H50N8O3
分子量
618.83 g/mol
Physical Properties
密度
1.26
化学标识符
SMILES
CCC1C(=O)N(C2=CN=C(N=C2N1C(C)C)NC3=C(C=C(C=C3)C(=O)NC4CCC(CC4)N5CCN(CC5)CC6CC6)OC)C
InChIKey
SXNJFOWDRLKDSF-STROYTFGSA-N
数据库引用
MDL号
MFCD20926414
常见问题
伏拉塞替为白色或类白色固体,熔点约为190-192℃。其分子量约为644.83 g/mol。该化合物在水中溶解度较低,在有机溶剂如二氯甲烷、乙腈中溶解度较高。其反应活性较高,易发生酰胺水解、环合等反应。
伏拉塞替可通过多步反应合成,通常包括环合、酰胺化、芳基化等步骤。首先通过环合反应得到环状化合物,然后通过酰胺化反应引入酰胺基团。最后通过芳基化反应引入苯环结构。具体合成方法和路线可能因文献而异,但通常需要催化剂和保护剂,反应产率约为80%-90%。
伏拉塞替主要用于医药行业,作为潜在的抗癌药物候选物。此外,由于其分子结构的特殊性,也可在聚合物合成、传感器和半导体材料等领域进行研究。
处理伏拉塞替时应佩戴合适的个人防护装备,如实验服、手套和护目镜。应在通风橱中操作,避免吸入粉尘或蒸气。如果不慎接触皮肤或眼睛,应立即用大量清水冲洗。若发生泄漏,应使用沙子或其他非可燃吸水材料清理,并及时通知专业人员。参考安全数据表(SDS)获取更详细的安全指导。
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
联系信息
邮箱
2030235803@qq.com

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