ChemicalBook--->CAS DataBase List--->2483-49-0

2483-49-0

2483-49-0 Structure

2483-49-0 Structure
IdentificationBack Directory
[Name]

BOC-ALA-ONP
[CAS]

2483-49-0
[Synonyms]

BOC-ALA-ONP
Boc-L-Ala-ONp
BOC-ALANINE-ONP
boc-ala-onp96+%
Boc-Ala-Onp, ≥98%
BOC-ALA-ONP USP/EP/BP
Boc-Ala-ONp Boc-Ala-ONp
Boc-Ala-ONp >=96.0% (HPLC)
(Tert-Butoxy)Carbonyl Ala-ONp
2-(3,5-dimethylphenyl)ethylurea
BOC-L-ALANINE-P-NITROPHENYL ESTER
BOC-L-ALANINE 4-NITROPHENYL ESTER
N-Boc-L-alanine p-nitrophenyl ester
N-Boc-L-Alanine 4-nitrophenyl ester
Boc-L-alanine-4-nitrophenyl ester99%
N-ALPHA-T-BOC-L-ALANINE-P-NITROPHENYL ESTER
Boc-Ala-ONp,Boc-L-alanine 4-nitrophenyl ester
N-tert-butyloxycarbonylalanine-4-nitrophenyl ester
N-TERT-BUTOXYCARBONYL-L-ALANINE-P-NITROPHENYL ESTER
N-(tert-butoxycarbonyl)-L-alanine 4-nitrophenyl ester
N-(tert-Butyloxycarbonyl)-L-alanine 4-nitrophenyl ester
4-nitrophenyl N-[(1,1-dimethylethoxy)carbonyl]-L-alaninate
4-nitrophenyl (2S)-2-{[(tert-butoxy)carbonyl]amino}propanoate
2-(tert-butoxycarbonylamino)propionic acid (4-nitrophenyl) ester
L-Alanine, N-[(1,1-dimethylethoxy)carbonyl]-, 4-nitrophenyl ester
(4-nitrophenyl) 2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoate
[EINECS(EC#)]

219-621-5
[Molecular Formula]

C14H18N2O6
[MDL Number]

MFCD00038117
[MOL File]

2483-49-0.mol
[Molecular Weight]

310.3
Chemical PropertiesBack Directory
[Melting point ]

78 °C(Solv: methanol (67-56-1))
[Boiling point ]

460.9±30.0 °C(Predicted)
[density ]

1.237±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[form ]

Powder
[pka]

10.87±0.46(Predicted)
[color ]

Pale brown
[Sensitive ]

Light Sensitive
[BRN ]

1892073
[Major Application]

peptide synthesis
[InChI]

1S/C14H18N2O6/c1-9(15-13(18)22-14(2,3)4)12(17)21-11-7-5-10(6-8-11)16(19)20/h5-9H,1-4H3,(H,15,18)/t9-/m0/s1
[InChIKey]

SUHFNHHZORGDFI-VIFPVBQESA-N
[SMILES]

C[C@H](NC(=O)OC(C)(C)C)C(=O)Oc1ccc(cc1)[N+]([O-])=O
Safety DataBack Directory
[WGK Germany ]

3
[F ]

8
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Uses]

peptide synthesis
[reaction suitability]

reaction type: Boc solid-phase peptide synthesis
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