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(3S)-4-[(2-Methyl-2-propanyl)oxy]-3-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)-4-oxobutanoic acid(CAS: 34582-32-6)
![(3S)-4-[(2-Methyl-2-propanyl)oxy]-3-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)-4-oxobutanoic acid](https://cnstatic.chemtradehub.com/structs/345/34582-32-6-ac7e.webp "(3S)-4-[(2-Methyl-2-propanyl)oxy]-3-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)-4-oxobutanoic acid")
CAS号
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基本信息
分子式
C13H23NO6
分子量
289.33 g/mol
Physical Properties
熔点
101.0 to 106.0 deg-C
沸点
429°C at 760 mmHg
闪点
213.3°C
化学标识符
SMILES
CC(C)(C)OC(=O)C(CC(=O)O)NC(=O)OC(C)(C)C
InChIKey
RAUQRYTYJIYLTF-QMMMGPOBSA-N
数据库引用
MDL号
MFCD00038272
Beilstein登记号
4191701
常见问题
Boc-L-天冬氨酸叔丁酯是一种白色结晶粉末，分子量约为244.37。它在水中的溶解度较低，在有机溶剂如乙腈、甲醇和氯仿中的溶解度较高。该化合物具有一定的反应活性，可以参与缩合、酯化等反应。
Boc-L-天冬氨酸叔丁酯通常通过将L-天冬氨酸与叔丁基对甲苯磺酸酯（TBO）进行反应合成。此反应在无水无氧条件下进行，使用硫酸或三氟乙酸作为催化剂，产率较高，选择性较好。
Boc-L-天冬氨酸叔丁酯主要应用于医药行业，作为合成药物的重要中间体。此外，它还用于聚合物合成、传感器制备以及半导体材料的制备等领域。
在处理Boc-L-天冬氨酸叔丁酯时，应穿戴适当的个人防护装备，如耐化学品手套、实验服和护目镜。操作应在通风橱中进行，避免吸入粉尘或蒸汽。如有泄露，应迅速清除并用大量水冲洗。参考安全数据表（SDS）获取详细信息。
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