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BOC-D-ALPHA-T-BUTYLGLYCINE

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CAS:124655-17-0
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CAS:124655-17-0
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Products Intro: Product Name:124655-17-0 BOC-D-ALPHA-T-BUTYLGLYCINE
CAS:124655-17-0
Purity:99% Package:25KG;5KG;1KG

BOC-D-ALPHA-T-BUTYLGLYCINE manufacturers

  • Boc-D-Tle-OH
  • Boc-D-Tle-OH pictures
  • $0.00/ kg
  • 2026-01-21
  • CAS:124655-17-0
  • Min. Order: 1kg
  • Purity: 98%
  • Supply Ability: 1T
BOC-D-ALPHA-T-BUTYLGLYCINE Basic information
Product Name:BOC-D-ALPHA-T-BUTYLGLYCINE
Synonyms:(R)-2-((tert-Butoxycarbonyl)aMino)-3,3-diMethylbutanoic acid;Boc-D-t-Leu;N-alpha-t-Butyloxycarbonyl-D-t-leucine, N-alpha-t-Butyloxycarbonyl-D-t-butylglycine;N-BOC-D-TERT-LEUCINE;(R)-2-(tert-butoxycarbonyl)-3,3-dimethylbutanoic a;BOC-TBU-D-GLY-OH;BOC-D-(TBU)GLY-OH;BOC-D-T-BUTYLGLYCINE
CAS:124655-17-0
MF:C11H21NO4
MW:231.29
EINECS:
Product Categories:Amino Acids;CHIRAL COMPOUNDS;Amino Acids & Deriv.;CHIRAL CHEMICALS;Peptide
Mol File:124655-17-0.mol
BOC-D-ALPHA-T-BUTYLGLYCINE Structure
BOC-D-ALPHA-T-BUTYLGLYCINE Chemical Properties
Melting point 118-121°C
Boiling point 350.0±25.0 °C(Predicted)
density 1.063±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
solubility slightly sol. in Methanol
pka4.03±0.10(Predicted)
form Solid
color White to Almost white
Optical RotationConsistent with structure
InChIInChI=1S/C11H21NO4/c1-10(2,3)7(8(13)14)12-9(15)16-11(4,5)6/h7H,1-6H3,(H,12,15)(H,13,14)/t7-/m0/s1
InChIKeyLRFZIPCTFBPFLX-ZETCQYMHSA-N
SMILESC(O)(=O)[C@@H](C(C)(C)C)NC(OC(C)(C)C)=O
CAS DataBase Reference124655-17-0(CAS DataBase Reference)
Safety Information
HazardClass IRRITANT
HS Code 2924190090
MSDS Information
BOC-D-ALPHA-T-BUTYLGLYCINE Usage And Synthesis
Chemical PropertiesWhite powder
UsesN-Boc-D-tert-leucine is a protected form of D-tert-leucine, and is used in the synthesis of primary amino acid derivatives (e.g. Desacetyl Desmethyl Lacosamide [D288325]) that possess anticonvulsant and neuropathic pain protection properties.
Synthesis
D-tert-Butylglycine

26782-71-8

Di-tert-butyl dicarbonate

24424-99-5

BOC-D-ALPHA-T-BUTYLGLYCINE

124655-17-0

General procedure for the synthesis of tert-butoxycarbonyl-D-tert-leucine from D-tert-leucine and di-tert-butyl dicarbonate: 3-methyl-D-valine (900 mg, 6.86 mmol) was dissolved in a mixture of 7 mL of a 1 M aqueous sodium hydroxide solution and 7 mL of methanol at 0°C, followed by the addition of di-tert-butyl dicarbonate (Boc-anhydride, 1.797 g, 8.23 mmol). The reaction mixture was gradually warmed to room temperature and stirred continuously overnight. Upon completion of the reaction, most of the methanol was removed by evaporation, and the reaction solution was acidified to pH 2 with 1 M aqueous HCl, followed by three extractions with ethyl acetate (3 × 20 mL). The organic phases were combined and washed twice with brine (2 × 5 mL). Finally, the solvent was removed by evaporation to afford tert-butoxycarbonyl-D-tert-leucine as a white solid in 83% yield (1.36 g). The product was characterized by NMR (400 MHz, DMSO-d6): δ 12.44 (1H, s), 6.82 (1H, d), 3.76 (1H, d), 1.38 (9H, s); UPLC analysis showed a retention time of 0.64 min and a molecular ion peak of 232 [M + H]+.

References[1] Patent: WO2011/69951, 2011, A1. Location in patent: Page/Page column 77
[2] Journal of Medicinal Chemistry, 2008, vol. 51, # 15, p. 4620 - 4631
[3] Journal of Medicinal Chemistry, 2011, vol. 54, # 13, p. 4815 - 4830
[4] Patent: WO2012/76877, 2012, A1. Location in patent: Page/Page column 97
[5] Patent: US2013/267510, 2013, A1. Location in patent: Paragraph 0708-0710
BOC-D-ALPHA-T-BUTYLGLYCINE Preparation Products And Raw materials
Raw materialsD-tert-Butylglycine-->Di-tert-butyl dicarbonate-->Water-->Sodium hydroxide-->Methanol
Preparation ProductsBoc-D-tert-Leucinol
Tag:BOC-D-ALPHA-T-BUTYLGLYCINE(124655-17-0) Related Product Information
N-Boc-D-Valino BOC-D-THR-OH N-Boc-L-valine Boc-D-Thr-Obzl Boc-beta-alanine N-(tert-Butoxycarbonyl)-L-alanine BOC-BETA-TBU-D-ALA-OH 4-(Aminocarbonyl)-N-[(1,1-dimethylethoxy)carbonyl]-2,6-dimethyl-L-phenylalanine (BOC-AMINOOXY)ACETIC ACID TERT-BUTOXY ACETIC ACID Boc-L-aspartic acid 4-tert-butyl ester Boc-D-aspartic acid 4-benzyl ester TERT-BUTYL N-ALLYLCARBAMATE BOC-ALA-GLY-OH BOC-HYP-OL N-Boc-L-Phenylalaninol N-Boc-exo-3-aminotropane BOC-D-Methionine

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