(4R,4aS,7aS,12bS)-3-(cyclopropylmethyl)-7-methylene-1,2,3,4,5,6,7,7a-octahydro-4aH-4,12-methanobenzofuro[3,2-e]isoquinoline-4a,9-diol hydrochloride(CAS: 58895-64-0)
![(4R,4aS,7aS,12bS)-3-(cyclopropylmethyl)-7-methylene-1,2,3,4,5,6,7,7a-octahydro-4aH-4,12-methanobenzofuro[3,2-e]isoquinoline-4a,9-diol hydrochloride (4R,4aS,7aS,12bS)-3-(cyclopropylmethyl)-7-methylene-1,2,3,4,5,6,7,7a-octahydro-4aH-4,12-methanobenzofuro[3,2-e]isoquinoline-4a,9-diol hydrochloride](https://cnstatic.chemtradehub.com/structs/588/58895-64-0-6c55.webp)
CAS号
相关产品
其他供应商提供的 (4R,4aS,7aS,12bS)-3-(cyclopropylmethyl)-7-methylene-1,2,3,4,5,6,7,7a-octahydro-4aH-4,12-methanobenzofuro[3,2-e]isoquinoline-4a,9-diol hydrochloride
基本信息
分子式
C21H26ClNO3
分子量
375.9 g/mol
Physical Properties
熔点
180-185°
化学标识符
SMILES
C=C1CCC2(C3CC4=C5C2(C1OC5=C(C=C4)O)CCN3CC6CC6)O.Cl
InChIKey
GYWMRGWFQPSQLK-OPHZJPRHSA-N
数据库引用
MDL号
MFCD07772293
常见问题
盐酸纳美芬是一种具有特定手性的化合物,属于多环芳香族化合物。它的分子量约为426.46 g/mol。盐酸纳美芬在水中具有一定的溶解度,在有机溶剂中的溶解度更高。其具有一定的反应活性,在酸碱条件下可能产生一定的变化。
盐酸纳美芬的合成通常涉及多个步骤,包括环化、氧化、还原等反应。常见的合成方法是从前体化合物出发,利用化学试剂如甲苯、溴化氢、催化剂如钯碳等进行环化和溴化反应,随后进行还原反应。该过程需要严格的温度控制和保护气体环境,以确保产物的纯度和选择性。
盐酸纳美芬主要用于医药行业,作为阿片类药物的拮抗剂,用于治疗阿片类药物引起的呼吸抑制。此外,在某些研究领域,它也被用于研究阿片受体的生物学功能。
在处理盐酸纳美芬时,应穿戴适当的个人防护装备,如实验室外套、手套和护目镜。操作应在通风橱中进行,以减少吸入或皮肤接触的风险。泄露时应立即使用吸水纸或沙子覆盖,并使用适当的吸收剂进行清理。操作过程中应避免高温和光照,以减少分解风险。建议查阅安全数据表(SDS)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


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