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Z-ABU-OH

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Company Name: Meryer (Shanghai) Chemical Technology Co., Ltd.  
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Company Name: Alfa Aesar  
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Company Name: GL Biochem (Shanghai) Ltd  
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Company Name: Shanghai Hanhong Scientific Co.,Ltd.  
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Z-ABU-OH manufacturers

  • Z-ABU-OH
  • Z-ABU-OH pictures
  • 2025-04-04
  • CAS:42918-86-5
  • Min. Order: 1kg
  • Purity: 98%
  • Supply Ability: 1Ton
  • Z-ABU-OH
  • Z-ABU-OH pictures
  • $7.00
  • 2019-07-06
  • CAS: 42918-86-5
  • Min. Order: 1kg
  • Purity: 99%
  • Supply Ability: 100kg
  • Z-ABU-OH
  • Z-ABU-OH pictures
  • $7.00
  • 2019-07-06
  • CAS:42918-86-5
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: 100kg
Z-ABU-OH Basic information
Product Name:Z-ABU-OH
Synonyms:(S)-Cbz-2-aMinobutyric acid;BENZYLOXYCARBONYL-L-2-AMINOBUTYRIC ACID;Z-D-Abu;Z-L-α-aminobutyric acid;Cbz-2-Abu-OH;Z-L-Abu-OH;Z-L-α-aminobutyric acid≥ 98% (HPLC);Z-2-ABU-OH
CAS:42918-86-5
MF:C12H15NO4
MW:237.25
EINECS:1533716-785-6
Product Categories:
Mol File:42918-86-5.mol
Z-ABU-OH Structure
Z-ABU-OH Chemical Properties
storage temp. Sealed in dry,2-8°C
solubility Soluble in water or 1% acetic acid
form Powder
AppearanceWhite to off-white Solid
Safety Information
MSDS Information
Z-ABU-OH Usage And Synthesis
Chemical PropertiesWhite crystalline powder
Uses(S)-Cbz-2-aminobutyric Acid can be used as inhibitors in treatment of gastrointestinal and mental disorders.
Synthesis
L(+)-2-Aminobutyric acid

1492-24-6

Benzyl chloroformate

501-53-1

Z-ABU-OH

42918-86-5

To benzyl chloroformate (17.06 mL, 119 mmol) was added slowly and dropwise (S)-2-aminobutyric acid (11.2 g, 109 mmol) solution of tetrahydrofuran (THF, 200 mL) and 2M aqueous sodium carbonate (65.2 mL, 130 mmol) at 0 °C. After dropwise addition, the reaction mixture was stirred at room temperature for 16 hours. After completion of the reaction, the aqueous layer was separated by extraction with H2O/tert-butyl methyl ether (TBME). The aqueous layer was acidified to pH=2 with 2M HCl aqueous solution and subsequently extracted with ethyl acetate (EtOAc). The organic layers were combined, dried with anhydrous sodium sulfate (Na2SO4), filtered and the filtrate was concentrated to afford (S)-2-(benzyloxycarbonylamino)butyric acid (22.8 g, 77% yield) as a colorless oil. The product could be used in the subsequent reaction without further purification.LC-MS analysis: [M-H] 236.2; retention time (Rt) 0.76 min (LCMS method 1).

References[1] Chemical and Pharmaceutical Bulletin, 1994, vol. 42, # 9, p. 1927 - 1930
[2] Patent: US2014/135330, 2014, A1. Location in patent: Paragraph 0230
[3] Journal of the American Chemical Society, 1964, vol. 86, p. 4991 - 4999
[4] Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation), 1964, p. 635 - 640
[5] Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1964, # 4, p. 685 - 692
Z-ABU-OH Preparation Products And Raw materials
Raw materialsL(+)-2-Aminobutyric acid-->Benzyl chloroformate-->Sodium carbonate-->Tetrahydrofuran-->Water
Tag:Z-ABU-OH(42918-86-5) Related Product Information
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