Benzofuro[4,3,2-efg][2]benzazocin-2-ol,2,3,3a,8,9,10,11,11b-octahydro-5-methoxy-9-methyl-, hydrobromide (9CI)(CAS: 69353-21-5)
![Benzofuro[4,3,2-efg][2]benzazocin-2-ol,2,3,3a,8,9,10,11,11b-octahydro-5-methoxy-9-methyl-, hydrobromide (9CI) Benzofuro[4,3,2-efg][2]benzazocin-2-ol,2,3,3a,8,9,10,11,11b-octahydro-5-methoxy-9-methyl-, hydrobromide (9CI)](https://cnstatic.chemtradehub.com/structs/693/69353-21-5-aa00.webp)
CAS号
相关产品
其他供应商提供的 Benzofuro[4,3,2-efg][2]benzazocin-2-ol,2,3,3a,8,9,10,11,11b-octahydro-5-methoxy-9-methyl-, hydrobromide (9CI)
基本信息
分子式
C17H22BrNO3
分子量
368.27 g/mol
化学标识符
SMILES
COc1ccc2c3c1OC1C3C(=CC(C1)O)CCN(C2)C.Br
InChIKey
DKGIHQCMWKXHHR-UHFFFAOYSA-N
数据库引用
MDL号
MFCD00067672
常见问题
左旋加兰他敏为白色或类白色结晶性粉末,分子量为415.42。该化合物不溶于水,可溶于乙醇等有机溶剂。其具有一定的反应活性,能够参与多种化学反应。
左旋加兰他敏通常通过多步合成路线制备,首先由苯甲醛和环戊酮等原料通过Knoevenagel缩合反应生成中间体,然后经过环化、还原等步骤最终得到目标化合物。常用的催化剂包括Pd/C等。产率约为70%。
左旋加兰他敏主要用于医药行业,作为一种治疗帕金森病的药物。此外,它还应用于聚合物合成中作为引发剂,以及在传感器和半导体行业作为特定功能材料。
处理左旋加兰他敏时,应佩戴适当的个人防护装备(PPE),如实验服、手套和护目镜。在通风橱中操作,避免吸入蒸气或粉尘。如发生泄漏,应迅速清理,并使用适当的清洁剂和防护措施。查阅物质安全数据表(MSDS)以获取详细的安全信息。
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
联系信息
邮箱
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电话
020-87687760
传真
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地址
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