BOC-(S)-3-氨基-4-(4-氯苯基)-丁酸
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- CAS号:
- 270596-42-4
- 英文名:
- BOC-(S)-3-AMINO-4-(4-CHLORO-PHENYL)-BUTYRIC ACID
- 英文别名:
- RARECHEM AK PT B071;Boc-b-HoPhe(4-Cl)-OH;Boc-β-HoPhe(4-Cl)-OH;Boc-β-HoPhe(4-Cl)-OH;BOC-L-Β-HOMO-4-CL-PHE;BOC-PHE(4-CL)-(C*CH2)OH;BOC-BETA-HOPHE(4-CL)-OH;Boc-L-β-HomoPhe(4-Cl)-OH;(s)-boc-4-chloro-β-homophe-oh;(S)-Boc-4-chloro-β-Homophe-OH
- 中文名:
- BOC-(S)-3-氨基-4-(4-氯苯基)-丁酸
- 中文别名:
- BOC-(S)-3-氨基-4-;BOC-4-氯-L-Β-高苯丙氨酸;(S)-BOC-4-氯-Β-高苯丙氨酸;BOC-L-Β-3-氨基-4-(4-氯苯基)-丁酸;BOC-(S)-3-氨基-4-(4-氯苯基)-丁酸;(S)-3-(BOC-氨基)-4-(4-氯苯基)丁酸;(S)-N-叔丁氧羰基-3-氨基-4-(4-氯苯基)丁酸;FMOC-(S)-3-AMINO-4-(4-CHLOROPHENYL)-BUTYRICACIDFMOC-S-3-氨基-4-(4-氯苯基)-丁酸
- CBNumber:
- CB8293936
- 分子式:
- C15H20ClNO4
- 分子量:
- 313.78
- MOL File:
- 270596-42-4.mol
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BOC-(S)-3-氨基-4-(4-氯苯基)-丁酸化学性质
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沸点:
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470.0±40.0 °C(Predicted)
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密度:
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1.220±0.06 g/cm3(Predicted)
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储存条件:
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Inert atmosphere,Room Temperature
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酸度系数(pKa):
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4.40±0.10(Predicted)
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CAS 数据库:
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270596-42-4(CAS DataBase Reference)
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BOC-(S)-3-氨基-4-(4-氯苯基)-丁酸性质、用途与生产工艺
BOC-(S)-3-氨基-4-(4-氯苯基)-丁酸是多肽合成中一个重要的起始反应物及关键中间体，其在多肽合成中得到广泛的应用。
(S)-3-氨基-4-(4-氯苯基)-丁酸为起始物料，经二碳酸二叔丁酯的氨基保护，制备得到目标化合物BOC-(S)-3-氨基-4-(4-氯苯基)-丁酸。BOC-(S)-3-氨基-4-(4-氯苯基)-丁酸的合成反应式如下图：
BOC-(S)-3-氨基-4-(4-氯苯基)-丁酸
上下游产品信息
上游原料
下游产品
| 更新日期 | 产品编号 | 产品名称 | CAS编号 | 包装 | 价格 |
|---|
| 2024/01/16 | XW0227059642404 | BOC-(S)-3-氨基-4-(4-氯苯基)丁酸 | 270596-42-4 | 5G | 1045元 |
| 2024/01/16 | XW0227059642403 | BOC-(S)-3-氨基-4-(4-氯苯基)丁酸 | 270596-42-4 | 1G | 209元 |
BOC-(S)-3-氨基-4-(4-氯苯基)-丁酸
生产厂家
270596-42-4, BOC-(S)-3-氨基-4-(4-氯苯基)-丁酸 相关搜索:
- B-Amino
- 3-Amino-4-phenylbutanoic Acid Analogs
- 3-Amino-4-phenylbutyric Acid Analogs
- 生化试剂
- 非天然氨基酸
- 合成
- Peptide Synthesis
- Specialty Synthesis
- Unnatural Amino Acid Derivatives
- Beta-Amino Acids
- 70596-42-4
- 27596-42-4
- FMOC-(S)-3-AMINO-4-(4-CHLOROPHENYL)-BUTYRICACIDFMOC-S-3-氨基-4-(4-氯苯基)-丁酸
- BOC-(S)-3-氨基-4-
- (S)-BOC-4-氯-Β-高苯丙氨酸
- (S)-3-(BOC-氨基)-4-(4-氯苯基)丁酸
- (S)-N-叔丁氧羰基-3-氨基-4-(4-氯苯基)丁酸
- BOC-4-氯-L-Β-高苯丙氨酸
- BOC-L-Β-3-氨基-4-(4-氯苯基)-丁酸
- BOC-(S)-3-氨基-4-(4-氯苯基)-丁酸
- 270596-42-4
- (S)-Boc-4-chloro-β-Homophe-OH
- (βS)-4-Chloro-β-[[(1,1-dimethylethoxy)carbonyl]amino]benzenebutanoic acid
- Boc-β-HoPhe(4-Cl)-OH
- (3S)-4-(4-chlorophenyl)-3-[(2-methylpropan-2-yl)oxycarbonylamino]butanoic acid
- (Tert-Butoxy)Carbonyl (S)-3-Amino-4-(4-chloro-phenyl)-butyric acid
- N-β-(t-Butoxycarbonyl)-4-chloro-L-β-homophenylalanine
- BOC-(S)-3-AMINO-4-(4-CHLORO-PHENYL)-BUTYRIC ACID USP/EP/BP
- Boc-(S)-3-amino-4-(4-chlorophenyl)-butyricaci
- Benzenebutanoic acid, 4-chloro-β-[[(1,1-dimethylethoxy)carbonyl]amino]-, (βS)-
- (3S)-3-{[(tert-butoxy)carbonyl]amino}-4-(4-chlorophenyl)butanoic acid
- Boc-L-3-Amino-4-(4-chlorophenyl)butyric acid
- Boc-L-β-HomoPhe(4-Cl)-OH
- Benzenebutanoic acid,4-chloro-b-[[(1,1-dimethylethoxy)carbonyl]amino]-,(bS)-
- (S)-4-Chloro-b-(Boc-amino)benzenebutanoic acid
- BOC-L-Β-HOMO-4-CL-PHE
- Boc-4-chloro-L-β-hoMophenylalanine
Boc-(S)-3-aMino-4-(4-chlorophenyl)butyric acid
- Boc-β-HoPhe(4-Cl)-OH
- Boc-4-chloro-L-β-homophenylalanine
- (S)-N-(tert-Butoxycarbonyl)-3-amino-4-(4-chlorophenyl)butyric acid
- (S)-3-((tert-Butoxycarbonyl)aMino)-4-(4-chlorophenyl)butanoic acid
- (S)-3-(Boc-amino)-4-(4-chlorophenyl)butyric acid, Boc-4-chloro-L-β-homophenylalanine
- Boc-b-HoPhe(4-Cl)-OH
- (s)-boc-4-chloro-β-homophe-oh
- BOC-PHE(4-CL)-(C*CH2)OH
- BOC-(S)-3-AMINO-4-(4-CHLORO-PHENYL)-BUTYRIC ACID
- BOC-(S)-3-AMINO-4-(4-CHLOROPHENYL)BUTANOIC ACID
- BOC-BETA-HOPHE(4-CL)-OH
- BOC-4-CHLORO-L-BETA-HOMOPHENYLALANINE
- (L)-3-BOC-AMINO-4-(4-CHLORO-PHENYL)-BUTYRIC ACID
- RARECHEM AK PT B071
- (S)-BOC-4-CHLORO-BETA-HOMOPHE-OH
- (S)-3-(BOC-AMINO)-4-(4-CHLOROPHENYL)BUTYRIC ACID
- N-T-BUTOXYCARBONYL-(S)-3-AMINO-4-(4-CHLOROPHENYL)BUTANOIC ACID
- N-BETA-T-BUTOXYCARBONYL-L-BETA-HOMO(4-CHLOROPHENYL)ALANINE