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Molecule
ID:38993
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₄H₁₈N₂O₆
Molecular Mass
310.30252
Exact Mass
310.11648631
Charge
0
InChI
InChI=1S/C14H18N2O6/c1-14(2,3)22-13(19)15-11(12(17)18)8-9-4-6-10(7-5-9)16(20)21/h4-7,11H,8H2,1-3H3,(H,15,19)(H,17,18)/t11-/m0/s1
InChIKey
XBQADBXCNQPHHY-NSHDSACASA-N
Canonic Smiles
OC(=O)[C@H](Cc1ccc(cc1)[N+](=O)[O-])NC(=O)OC(C)(C)C
Isomeric Smiles
c1(ccc(cc1)C[C@@H](C(=O)O)NC(=O)OC(C)(C)C)[N+](=O)[O-]
Calculated Properties
JChem
Acid pKa
3.3160481
H Acceptors
5
H Donor
2
LogD (pH = 5.5)
0.3420817
LogD (pH = 7.4)
-0.91295594
Log P
2.5096967
Molar Refractivity
76.3098
Polarizability
29.477247
Polar Surface Area
118.77
Rotatable Bonds
7
Lipinski's Rule of Five
true
Data Source
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Names and Identifiers
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Registration numbers
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Properties
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Related Proteins
No Data Available
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Molecular Spectra
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Molecule Details
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References
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Bioactivity
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General Information
Calculated Properties
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RDKit
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JChem
Data Source
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Academic Data
Names and Identifiers
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IUPAC Traditional name
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IUPAC name
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Synonyms
Registration numbers
Properties
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Safety Information
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Product Information
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Physical Property
Related Proteins
Molecular Spectra
Molecule Details
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Sigma Aldrich
References
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PubChem Literature
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
OR14584
Sigma Aldrich
15348
B8390
Alfa Aesar
H51986
Matrix Scientific
041892
Academic Data
PubChem
7021882
Names and Identifiers
IUPAC Traditional name
(2S)-2-[(tert-butoxycarbonyl)amino]-3-(4-nitrophenyl)propanoic acid
IUPAC name
(2S)-2-{[(tert-butoxy)carbonyl]amino}-3-(4-nitrophenyl)propanoic acid
Synonyms
Boc-4-nitro-L-phenylalanine
4-Nitro-L-phenylalanine, N-BOC protected
Boc-4-nitro-L-phenylalanine
Boc-L-4-硝基苯丙氨酸
Boc-Phe(4-NO2)-OH
N-Boc-4-nitro-L-phenylalanine
Boc-Phe(4-NO2)-OH
N-Boc-4-硝基-L-苯基丙氨酸
Registration numbers
MDL Number
MFCD00038128
Beilstein Number
2820671
EC Number
251-450-1
CAS Number
33305-77-0
PubChem CID
7021882
PubChem SID
161002300
24849347
Molecule Details
Sigma Aldrich
15348
Packaging
1, 5 g in glass bottle
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Registration numbers
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MDL Number
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Beilstein Number
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EC Number
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CAS Number
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PubChem CID
•
PubChem SID
Properties
Safety Information
MSDS Link
Download link
Source
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Source
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Source
TSCA Listed
false
Source
否
Source
IRRITANT
Source
Irritant
Source
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
3
Source
-20°C
Source
Product Information
≥99.0% (T)
Source
95%
Source
C14H18N2O6
Source
Physical Property
[α]20/D +8±1°, c = 1% in methanol
Source
+8 (c=1 in methanol)
Source
Storage Warning
Personal Protective Equipment
German water hazard class
Storage Temperature
Purity
Empirical Formula (Hill Notation)
Optical Rotation