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BOC-D-TRYPTOPHANOL

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Company Name: J & K SCIENTIFIC LTD.  
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BOC-D-TRYPTOPHANOL manufacturers

  • BOC-D-TRYPTOPHANOL
  • BOC-D-TRYPTOPHANOL pictures
  • 2026-03-20
  • CAS:158932-00-4
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: 20 mt
  • N-t-BOC-D-Tryptophanol
  • N-t-BOC-D-Tryptophanol pictures
  • $100.00
  • 2024-04-24
  • CAS:158932-00-4
  • Min. Order: 1kg
  • Purity: 99.93%
  • Supply Ability: 1000kg per week
  • BOC-D-TRYPTOPHANOL
  • BOC-D-TRYPTOPHANOL pictures
  • $50.00
  • 2023-08-11
  • CAS:158932-00-4
  • Min. Order: 1kg
  • Purity: 99.9%
  • Supply Ability: 10000MT
BOC-D-TRYPTOPHANOL Basic information
Product Name:BOC-D-TRYPTOPHANOL
Synonyms:BOC-(R)-2-AMINO-3-(3-INDOLYL)-1-PROPANOL;BOC-D-TRYPTOPHANOL;BOC-D-TRP-OL;N-BOC-D-TRYPTOPHANOL;N-ALPHA-T-BOC-D-TRYPTOPHANOL;N-T-BOC-D-TRYPTOPHANOL;N-alpha-t-Butyloxycarbonyl-D-tryptophanol;(R)-tert-Butyl (1-hydroxy-3-(1H-indol-3-yl)propan-2-yl)carbaMate
CAS:158932-00-4
MF:C16H22N2O3
MW:290.36
EINECS:
Product Categories:
Mol File:158932-00-4.mol
BOC-D-TRYPTOPHANOL Structure
BOC-D-TRYPTOPHANOL Chemical Properties
Melting point 119-121℃
Boiling point 518.1±45.0 °C(Predicted)
density 1.190
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
form Powder
pka12.06±0.46(Predicted)
AppearanceWhite to off-white Solid
Safety Information
HS Code 2933499090
MSDS Information
BOC-D-TRYPTOPHANOL Usage And Synthesis
Chemical PropertiesWhite solid
Synthesis
N-[(tert-Butoxy)carbonyl]-D-tryptophan

5241-64-5

BOC-D-TRYPTOPHANOL

158932-00-4

General procedure for the synthesis of N-Boc-D-tryptophan from Boc-D-tryptophan: a) Synthesis of compound 22; Compound 1 (Boc-D-tryptophan, 10.0 g, 33 mmol) was dissolved in THF (50 mL), cooled to 0 °C under nitrogen atmosphere, and then BH3/THF solution was slowly added dropwise. The reaction mixture was gradually warmed to room temperature and stirred continuously for 16 hours. Upon completion of the reaction, the reaction was quenched with aqueous potassium carbonate and subsequently extracted with ethyl acetate (100 mL x 3). The organic phases were combined, washed with brine (50 mL), dried over anhydrous sodium sulfate and concentrated under reduced pressure. Purification by column chromatography (petroleum ether/ethyl acetate=4:1) afforded the product 22 (N-Boc-D-chromanol) as a white solid (5.72 g, 60% yield).1H NMR (400 MHz, CDCl3): δ1.46 (s, 9H), 3.02 (d, J=6.8 Hz, 2H), 3.80-3.55 (m, 2H). 4.10-3.95 (m, 1H), 4.86 (br s, 1H), 7.07 (s, 1H), 7.16 (t, J=7.2Hz, 1H), 7.23 (t, J=7.2Hz, 1H), 7.39 (d, J=8.4Hz, 1H), 7.68 (d, J=7.6Hz, 1H), 8.20 (s, 1H).

References[1] ChemMedChem, 2016, p. 1924 - 1935
[2] Patent: WO2012/55945, 2012, A1. Location in patent: Page/Page column 23
[3] Journal of Medicinal Chemistry, 1994, vol. 37, # 13, p. 2011 - 2032
BOC-D-TRYPTOPHANOL Preparation Products And Raw materials
Raw materialsN-[(tert-Butoxy)carbonyl]-D-tryptophan-->Water-->Potassium carbonate-->Tetrahydrofuran-->BORANE THF
Tag:BOC-D-TRYPTOPHANOL(158932-00-4) Related Product Information
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