ChemicalBook--->CAS DataBase List--->15761-38-3

15761-38-3

15761-38-3 Structure

15761-38-3 Structure
IdentificationMore
[Name]

N-(tert-Butoxycarbonyl)-L-alanine
[CAS]

15761-38-3
[Synonyms]

BOC-ALA
BOC-ALANINE
BOC-ALA-OH
BOC-L-ALA
BOC-L-ALANINE
BOC-L-ALANINE-OH
BOC-L-ALA-OH
H-ALPHA-T-BOC-L-ALANINE
L-ALANINE, N-[(1,1-DIMETHYLETHOXY)CARBONYL]-
N-[(1,1-Dimethylethoxy)carbonyl]-L-alanine
N-ALPHA-T-BOC-L-ALANINE
N-ALPHA-T-BUTYLOXYCARBONYL-L-ALANINE
N-ALPHA-TERT-BUTYLOXYCARBONYL-L-ALANINE
N-BOC-L-ALANINE
N-T-BOC-L-ALANINE
N-(T-BUTOXYCARBONYL)-L-ALANINE
N-(TERT-BUTOXYCARBONYL)-L-ALANINE
N-(TERT-BUTOXYEARBONYL)-L-ALANINE
TBOC-L-ALANINE
T-BUTYLOXYCARBONYL-L-ALANINE
[EINECS(EC#)]

239-847-8
[Molecular Formula]

C8H15NO4
[MDL Number]

MFCD00037225
[Molecular Weight]

189.21
[MOL File]

15761-38-3.mol
Chemical PropertiesBack Directory
[Appearance]

White to off-white microcrystalline powder
[Melting point ]

79-83 °C(lit.)
[alpha ]

-26 º (c=2, acetic acid)
[Boiling point ]

324.46°C (rough estimate)
[density ]

1.2321 (rough estimate)
[refractive index ]

-25.5 ° (C=2, AcOH)
[storage temp. ]

−20°C
[solubility ]

DMSO, Methanol
[form ]

Granular Powder
[pka]

4.02±0.10(Predicted)
[color ]

White
[Optical Rotation]

[α]20/D 25±1°, c = 2% in acetic acid
[Detection Methods]

T,NMR
[BRN ]

1726365
[Major Application]

peptide synthesis
[InChI]

InChI=1S/C8H15NO4/c1-5(6(10)11)9-7(12)13-8(2,3)4/h5H,1-4H3,(H,9,12)(H,10,11)/t5-/m0/s1
[InChIKey]

QVHJQCGUWFKTSE-YFKPBYRVSA-N
[SMILES]

C(O)(=O)[C@H](C)NC(OC(C)(C)C)=O
[CAS DataBase Reference]

15761-38-3(CAS DataBase Reference)
[EPA Substance Registry System]

15761-38-3(EPA Substance)
Questions And AnswerBack Directory
[Synthesis]

Under stirring at room temperature, 2 N sodium hydroxide aqueous solution was added to a suspension of S-alanine (1.0 equivalent) in a mixture of dioxane and water (1:1, 100 mL). The resulting reaction mixture was transferred to an ice-water bath and cooled to 0 °C, then stirred for 15 min. A solution of (Boc)₂O (1.1 equivalent) in dioxane (10 mL) was then added to the reaction mixture, and the mixture was stirred at 0 °C for another 45 min. The ice bath was removed, and the reaction mixture was brought to room temperature. The completion of the reaction was monitored by TLC. After the reaction was complete, the reaction mixture was concentrated under reduced pressure, and the aqueous layer was acidified with citric acid (pH 2-3). The mixture was extracted three times with ethyl acetate, and all organic layers were combined and washed three times with brine. The organic layers were separated and dried on Na₂SO₄. The desiccant was removed by filtration, and the filtrate was concentrated under reduced pressure to obtain N-tert-butoxycarbonyl-L-alanine.

Synthetic Route of N-tert-Butoxycarbonyl-L-Alanine

Figure: Synthetic Route of N-tert-Butoxycarbonyl-L-Alanine

Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[Hazard Codes ]

Xi,Xn
[Risk Statements ]

R20/21/22:Harmful by inhalation, in contact with skin and if swallowed .
R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S24/25:Avoid contact with skin and eyes .
S36:Wear suitable protective clothing .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
[WGK Germany ]

3
[TSCA ]

Yes
[REACH Registrations]

Active
[HazardClass ]

IRRITANT
[HS Code ]

29241990
[Storage Class]

11 - Combustible Solids
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

BOC-L-Alanine(15761-38-3).msds
Hazard InformationBack Directory
[Chemical Properties]

White to off-white microcrystalline powder
[Uses]

Boc-Ala-OH can be used:
  • In the preparation of N-propargylalanine, a key precursor to generate N-(3-aryl)propylated alanine residues.
  • In the resolution of racemic mixture of 3,3′-bis(benzyloxy)-1,1′-binaphthalene-2,2′-diol.
  • In the one-pot synthesis of hybrid tripeptidomimetics containing both amide and imide functionalities.

[reaction suitability]

reaction type: Boc solid-phase peptide synthesis
reaction type: C-H Activation
reagent type: ligand
reaction type: Peptide Synthesis
Spectrum DetailBack Directory
[Spectrum Detail]

N-(tert-Butoxycarbonyl)-L-alanine(15761-38-3)MS
N-(tert-Butoxycarbonyl)-L-alanine(15761-38-3)1HNMR
N-(tert-Butoxycarbonyl)-L-alanine(15761-38-3)IR1
N-(tert-Butoxycarbonyl)-L-alanine(15761-38-3)IR2
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

BOC-L-Alanine, 99+%(15761-38-3)
[Alfa Aesar]

N-Boc-L-alanine, 98+%(15761-38-3)
[Sigma Aldrich]

15761-38-3(sigmaaldrich)
[TCI AMERICA]

N-(tert-Butoxycarbonyl)-L-alanine,>98.0%(LC)(T)(15761-38-3)
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