BOC-ALA-NH2

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CAS:85642-13-3
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CAS:85642-13-3
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CAS:85642-13-3
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CAS:85642-13-3
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Products Intro: Product Name:Boc-Ala-NH2
CAS:85642-13-3
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BOC-ALA-NH2 manufacturers

  • BOC-ALA-NH2
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  • $15.00 / 1Kg/Bag
  • 2023-04-12
  • CAS:85642-13-3
  • Min. Order: 1Kg/Bag
  • Purity: 98%
  • Supply Ability: Weekly supply of 1000 KG
  • BOC-ALA-NH2
  • BOC-ALA-NH2 pictures
  • $2.00 / 1kg
  • 2019-07-06
  • CAS:85642-13-3
  • Min. Order: 1kg
  • Purity: 99%
  • Supply Ability: ask
BOC-ALA-NH2 Basic information
Product Name:BOC-ALA-NH2
Synonyms:BOC-Beta-ala-NH2;N-alpha-t-Butyloxycarbonyl-beta-alanine amide;N-t-Butyloxycarbonyl-L-alanine amide;Boc-L-alanine amide;BOC-L-ALA-NH2;BOC-ALA-NH2;N-tert-Butoxycarbonyl-L-alanine amide;tert-butyl (1S)-2-amino-1-methyl-2-oxoethylcarbamate
CAS:85642-13-3
MF:C8H16N2O3
MW:188.22
EINECS:1533716-785-6
Product Categories:
Mol File:85642-13-3.mol
BOC-ALA-NH2 Structure
BOC-ALA-NH2 Chemical Properties
Melting point 124-125 °C
Boiling point 343.1±25.0 °C(Predicted)
density 1.081±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
solubility Soluble in water or 1% acetic acid
pka11.38±0.46(Predicted)
form Solid
AppearanceWhite to off-white Solid
Optical Rotation-34.8°(C=0.01g/mI, CHCL3, 20°C, 589nm)
Water Solubility Soluble in water or 1% acetic acid.
Safety Information
MSDS Information
BOC-ALA-NH2 Usage And Synthesis
UsesN-Boc-L-alaninamide is used as pharmaceutical intermediate.
Synthesis
N-(tert-Butoxycarbonyl)-L-alanine

15761-38-3

BOC-D-ALA-NH2

78981-25-6

GENERAL STEPS: N-Boc-L-alanine (5.0 g, 26.4 mmol) was dissolved in anhydrous THF at -10 °C and triethylamine (3 mL, 21.12 mmol) and ethyl chloroformate (2.5 mL, 26.4 mmol) were added sequentially under stirring. The reaction mixture was continued to be stirred at this temperature for 1 hour. Subsequently, ammonia (NH3) was passed into the reaction system for 1.5 hours. The reaction mixture was brought to room temperature and stirred overnight. After completion of the reaction, the THF solvent was removed by distillation under reduced pressure. Saturated sodium chloride solution (40 mL) was added to the residue and extracted with ethyl acetate (5 x 40 mL). The organic phases were combined, washed with 0.5 M hydrochloric acid (2 x 30 mL), dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give N-Boc-D-alaninamide.

References[1] Tetrahedron, 1999, vol. 55, # 42, p. 12301 - 12308
[2] Tetrahedron Letters, 2007, vol. 48, # 4, p. 603 - 607
[3] Synthetic Communications, 2013, vol. 43, # 7, p. 993 - 1006
[4] Bulletin of the Chemical Society of Japan, 1988, vol. 61, # 7, p. 2647 - 2648
[5] Tetrahedron Asymmetry, 2013, vol. 24, # 24, p. 1572 - 1575
BOC-ALA-NH2 Preparation Products And Raw materials
Raw materialsN-(tert-Butoxycarbonyl)-L-alanine-->BOC-L-ALANINE METHYL ESTER-->Triethylamine-->Ethyl chloroformate-->Ammonia
Tag:BOC-ALA-NH2(85642-13-3) Related Product Information
N-(tert-Butoxycarbonyl)-L-alanine BOC-GLU-GLU-LEU-OME BOC-ALA-ALA-PNA BOC-GLN-ARG-ARG-AMC ACETATE SALT BOC-MET-LEU-PHE-OH N-T-BOC-LEU-GLY-ARG P-NITROANILIDE BOC-PHE-PHE-GLY-OH BOC-PRO-LEU-VAL-OME BOC-LEU-GLY-ARG-AMC ACETATE SALT BOC-ILE-GLY-OH BOC-ALA-ALA-OH BOC-GLU-LYS-LYS-MCA BOC-VAL-PRO-ARG-MCA BOC-PRO-PRO-OH BOC-PHE-SER-ARG-AMC ACETATE SALT BOC-VAL-PRO-ARG-AMC HCL BOC-VAL-LEU-LYS-AMC ACETATE BOC-HIS-NHNH2

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