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Home > Encyclopedia > 2-(9H-Fluoren-9-ylmethoxycarbonylamino)-3-hydroxy-butanoic acid

2-(9H-Fluoren-9-ylmethoxycarbonylamino)-3-hydroxy-butanoic acid

2-(9H-Fluoren-9-ylmethoxycarbonylamino)-3-hydroxy-butanoic acid structure

2-(9H-Fluoren-9-ylmethoxycarbonylamino)-3-hydroxy-butanoic acid 

structure
  • CAS No:

    73731-37-0

  • Formula:

    C19H19NO5

  • Chemical Name:

    2-(9H-Fluoren-9-ylmethoxycarbonylamino)-3-hydroxy-butanoic acid

  • Synonyms:

    FMOC-L-THREONINE extrapure;N-(9-Fluorenylmethoxycarbonyl)-L-threonine ,99%;N-alpha-(9-fluorenylmethyloxycarbonylamino)-3-hydroxybutanoic acid;Fmoc-L-threonine ,99%;Fmoc-L-Threonine monohydrate ,99%;Fmoc-Threonine-OH;2-(9H-Fluoren-9-ylMethoxycarbony-laMino)-3-;FMoc-Thr-OH·H2O FMoc-L-threonine Monohydrate

  • Categories:

    Pharmaceutical Intermediates  >  Antibacterials

Description

White powder

2-(9H-Fluoren-9-ylmethoxycarbonylamino)-3-hydroxy-butanoic acid Basic Attributes

341.36

341.126312

1533716-785-6

334300

DTXSID60513242

2924299090

Characteristics

95.9

2.4

White to off-white crystalline powder

1.3±0.1 g/cm3

115°C(dec.)

596.5°C at 760 mmHg

314.6±30.1 °C

1.618

2-8°C

-16 º (c=1%, DMF)

Safety Information

NONH for all modes of transport

3

36/37/38

22-24/25-26

Xi

2-(9H-Fluoren-9-ylmethoxycarbonylamino)-3-hydroxy-butanoic acid Use and Manufacturing

Methods of Manufacturing

At r.t. a solution of FmocONSu (3.37 g, 10.0 mmol) in 25 mL of DioxaneGeneral procedure: To a solution of H-Phe-OH (100 mg, 60.5 mmol) in 50 percent MeCN (6.1 mL)were added Fmoc-OPhth (233 mg, 60.5 mmol) and K2CO3 (167 mg, 121 mmol) and stirred at room temperature. After 2 h of stirring saturated sodium bicarbonate solution and H2O were added and the resulting solution was washed with diethyl ether. The aqueous phase is acidified to pH 1 with 1M HCl and extracted with diethyl ether. The organic phase was washed with 1 M HCl, H2O, brine, dried over MgSO4. The filtrate was evaporatedevaporated under reduced pressure to give yellow solid as crude product.

Uses

Used in biochemical reagents and peptide synthesis.

Computed Properties

Molecular Weight:341.4
XLogP3:2.4
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:6
Exact Mass:341.12632271
Monoisotopic Mass:341.12632271
Topological Polar Surface Area:95.9
Heavy Atom Count:25
Complexity:474
Undefined Atom Stereocenter Count:2
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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