2,2'-[(5-Butyryl-2,4,6-trihydroxy-1,3-phenylene)bis(methylene)]bis(6-acetyl-3,5-dihydroxy-4,4-dimethyl-2,5-cyclohexadien-1-one)(CAS: 38226-84-5)
![2,2'-[(5-Butyryl-2,4,6-trihydroxy-1,3-phenylene)bis(methylene)]bis(6-acetyl-3,5-dihydroxy-4,4-dimethyl-2,5-cyclohexadien-1-one) 2,2'-[(5-Butyryl-2,4,6-trihydroxy-1,3-phenylene)bis(methylene)]bis(6-acetyl-3,5-dihydroxy-4,4-dimethyl-2,5-cyclohexadien-1-one)](https://cnstatic.chemtradehub.com/structs/382/38226-84-5-a669.webp)
CAS号
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其他供应商提供的 2,2'-[(5-Butyryl-2,4,6-trihydroxy-1,3-phenylene)bis(methylene)]bis(6-acetyl-3,5-dihydroxy-4,4-dimethyl-2,5-cyclohexadien-1-one)
基本信息
分子式
C32H36O12
分子量
612.63 g/mol
物理状态
Yellow powder
化学标识符
SMILES
CCCC(=O)c1c(c(c(c(c1O)CC2=C(C(C(=C(C2=O)C(=O)C)O)(C)C)O)O)CC3=C(C(C(=C(C3=O)C(=O)C)O)(C)C)O)O
InChIKey
ABMAWOVWVRXUCA-UHFFFAOYSA-N
数据库引用
MDL号
MFCD20527290
常见问题
绵马酸ABA是一种结晶性化合物,具有较高的结晶度。其分子量为632.6 g/mol。绵马酸ABA在水中的溶解度较低,在一些有机溶剂中如乙醇、丙酮中具有较好的溶解性。其具有一定的反应活性,可以参与多种有机化学反应,如酯化、氧化反应等。
绵马酸ABA通常通过一系列有机合成步骤制备。首先,以苯甲醛为原料,在铜催化剂的作用下进行选择性氧化生成苯甲酸。然后,将苯甲酸与相应的酯化试剂反应,得到中间体。进一步通过多步反应,最终得到绵马酸ABA。此过程中需要严格控制反应条件,以确保产率和选择性。
绵马酸ABA主要应用于医药行业,作为药物中间体用于合成某些药物。此外,由于其特殊的化学结构,也可以在聚合物、传感器、半导体等领域有一定的应用潜力,但具体应用仍需进一步研究验证。
在处理绵马酸ABA时,应穿戴适当的个人防护装备,如实验服、手套和护目镜。工作应在通风橱中进行,避免吸入粉尘或蒸汽。不慎接触皮肤或眼睛应立即用大量清水冲洗。若发生泄露,应立即清理,避免污染环境。详细的安全数据表(SDS)可提供更全面的安全指导。
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

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