ChemicalBook > CAS DataBase List > BOC-DL-MET-OH

BOC-DL-MET-OH

Product Name
BOC-DL-MET-OH
CAS No.
93000-03-4
Chemical Name
BOC-DL-MET-OH
Synonyms
Boc-DL-Met;BOC-DL-MET-OH;BOC-DL-METHIONINE;N-Boc-DL-methionine;Boc-DL-methionine99%;BOC-DL-MET-OH USP/EP/BP;N-Boc-DL-Methionine, ≥98%;(tert-Butoxycarbonyl)methionine;N-T-BUTOXYCARBONYL-DL-METHIONINE;N-tert-Butoxycarbonyl-DL-methionine
CBNumber
CB1766237
Molecular Formula
C10H19NO4S
Formula Weight
249.33
MOL File
93000-03-4.mol
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BOC-DL-MET-OH Property

Boiling point:
415.5±40.0 °C(Predicted)
Density 
1.160±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,2-8°C
form 
Solid
pka
3.83±0.10(Predicted)
color 
White to off-white
CAS DataBase Reference
93000-03-4
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Safety

HS Code 
29309090
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
B658965
Product name
BOC-DL-Met-OH
Packaging
100mg
Price
$60
Updated
2021/12/16
Usbiological
Product number
236273
Product name
Boc-DL-methionine 99+%
Packaging
5g
Price
$186
Updated
2021/12/16
Usbiological
Product number
264886
Product name
Boc-DL-methionine
Packaging
10g
Price
$343
Updated
2021/12/16
Chem-Impex
Product number
04004
Product name
Boc-DL-methionine,≥99%(HPLC)
Purity
≥99%(HPLC)
Packaging
5G
Price
$36.22
Updated
2021/12/16
Biosynth Carbosynth
Product number
FB47930
Product name
Boc-DL-methionine
Packaging
5G
Price
$60
Updated
2021/12/16
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BOC-DL-MET-OH Chemical Properties,Usage,Production

Uses

(tert-Butoxycarbonyl)methionine is a Methionine.html" class="link-product" target="_blank">Methionine (HY-13694) derivative[1].

Synthesis

24424-99-5

59-51-8

93000-03-4

General procedure for the synthesis of 2-((tert-butoxycarbonyl)amino)-4-(methylthio)butanoic acid from di-tert-butyl dicarbonate and DL-methionine: DL-methionine (20 g, 0.134 mol) was dissolved in 250 mL of a 10% aqueous sodium carbonate solution and cooled to 0 °C. A solution of di-tert-butyl dicarbonate (32.17 g, 0.147 mol) dissolved in 100 mL of dioxane was slowly added dropwise over a period of 1 hour. After the dropwise addition was completed, the cooling bath was removed and the reaction mixture was stirred at room temperature overnight. Upon completion of the reaction, about half of the solvent was removed by evaporation under reduced pressure. The reaction mixture was cooled with an ice bath and the pH was adjusted to 2-3 with 10% aqueous citric acid.The aqueous phase was extracted with ethyl acetate (3 x 200 mL) and the organic layers were combined and washed sequentially with 200 mL of water and 200 mL of saturated saline (2 x 200 mL). The organic layer was dried with anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue was ground with mixed solvent ethyl acetate-petroleum ether at -20 °C to give the pure product 2-((tert-butoxycarbonyl)amino)-4-(methylthio)butanoic acid (28 g, 84% yield). The product was a white solid with a melting point of 88-90 °C (literature value 87-91 °C). Thin layer chromatography (TLC) Rf = 0.67 (unfolding agent S4).1H NMR (600 MHz, CDCl3) δ: 5.27 (br s, 1H, NH), 4.45 (m, 1H), 2.58 (t, J = 7.5 Hz, 2H), 2.18 (m, 1H), 2.11 (s, 3H, SCH3), 1.98 (m, 1H). 1.45 (s, 9H, t-Bu).13C NMR (150.9 MHz, CDCl3) δ: 176.91 (COOH), 155.60 (NCOO), 80.32, 52.73, 31.86, 29.93, 28.24 (3C), 15.32.IR (KBr) νmax (cm-1): 3380 ( NH), 3500-2800 (br, COOH), 1715 (C=O, acid), 1673 (C=O, carbamate), 1543 (amide II), 2977 (s), 1368 (m, CH3). High resolution mass spectrometry (HRMS-ESI) calculated value C10H19O4NNaS [M+Na]+: 272.09270, measured value: 272.09281.

References

[1] Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144. DOI:10.1080/10408398.2012.708368

BOC-DL-MET-OH Preparation Products And Raw materials

Raw materials

Preparation Products

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View Lastest Price from BOC-DL-MET-OH manufacturers

Career Henan Chemical Co
Product
BOC-DL-MET-OH 93000-03-4
Price
US $1.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
20kg
Release date
2018-08-16

93000-03-4, BOC-DL-MET-OHRelated Search:


  • N-[(1,1-Dimethylethoxy)Carbonyl]-Methionine
  • N-tert-Butoxycarbonyl-DL-methionine
  • BOC-DL-METHIONINE
  • BOC-DL-MET-OH
  • N-T-BUTOXYCARBONYL-DL-METHIONINE
  • Boc-DL-methionine99%
  • N-Boc-DL-methionine
  • Boc-DL-Met
  • (tert-Butoxycarbonyl)methionine
  • N-Boc-DL-Methionine, ≥98%
  • 2-{[(tert-butoxy)carbonyl]amino}-4-(methylsulfanyl)butanoic acid
  • 2-[(2-methylpropan-2-yl)oxycarbonylamino]-4-methylsulfanylbutanoicaci
  • BOC-DL-MET-OH USP/EP/BP
  • Methionine, N-[(1,1-dimethylethoxy)carbonyl]-
  • (tert-Butoxycarbonyl)methionine - [B92213]
  • 93000-03-4