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- 天鸿
- 泰州
- 140
- 2025年07月09日
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- 详细信息
- 文献和实验
- 技术资料
- 保质期：
3年
- 英文名：
Cbz-AIB-OH,
- 库存：
1吨
- 供应商：
泰州天鸿生化科技有限公司
| 项目Item | 检测标准Test Criterion | 结果Result |
| 外观Appearance | 白色结晶粉末 white crystalline powder |
符合Conforms |
| 含量Assay | min 99.0% | 99.6% |
| 熔点Melting Point | 63~68℃ | 64.7℃ |
| 干燥失重Loss on drying | max 0.5% | 0.23% |
| 灼烧残渣Residue on Ignition | max 0.4% | 0.1% |
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文献和实验CarbonCarbon Bond-Forming Enzymes for the Synthesis of Non-natural Amino Acids
An enzymatic methodology for the preparation of β-hydroxy-α-amino acid derivatives is described. The method consists of the stereoselective aldol addition reaction of glycine to N -Cbz-amino aldehydes furnishing 3-hydroxy-2,4-diaminobutyric
Synthesis of Cbz-Protected Ketomethylene Dipeptide Isosteres
1 are chemically characterized by a 1,4-disposition of the carbonyl groups (ketone and carboxylate) and have an alkyl group at C-2 that is a chiral center. Protecting groups at amino nitrogen (typically carbamate such as Cbz or Boc) and the carboxyl group
Methylated Polyamines as Research Tools
resulted in corresponding di-Boc-amines, which after deprotection gave target β- and γ-MeSpd’s. To prepare α-MeSpd, the starting compound, 3-amino-1-butanol, was converted into N -Cbz-3-amino-1-butyl methanesulfonate, which alkylated putrescine
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