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Molecule
ID:38969
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₅H₂₁NO₄
Molecular Mass
279.33154
Exact Mass
279.14705816
Charge
0
InChI
InChI=1S/C15H21NO4/c1-10-6-5-7-11(8-10)9-12(13(17)18)16-14(19)20-15(2,3)4/h5-8,12H,9H2,1-4H3,(H,16,19)(H,17,18)/t12-/m1/s1
InChIKey
HBBXWMALJNZDOM-GFCCVEGCSA-N
Canonic Smiles
O=C(OC(C)(C)C)N[C@@H](C(=O)O)Cc1cccc(c1)C
Isomeric Smiles
c1c(cc(cc1)C[C@H](C(=O)O)NC(=O)OC(C)(C)C)C
Calculated Properties
JChem
Acid pKa
4.1369863
H Acceptors
3
H Donor
2
LogD (pH = 5.5)
1.7046403
LogD (pH = 7.4)
0.007808175
Log P
3.083134
Molar Refractivity
75.0305
Polarizability
29.25822
Polar Surface Area
75.63
Rotatable Bonds
6
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
No Data Available
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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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Commercial Catalog
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Academic Data
Names and Identifiers
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Synonyms
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IUPAC Traditional name
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IUPAC name
Registration numbers
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PubChem SID
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MDL Number
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CAS Number
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PubChem CID
Properties
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Safety Information
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Product Information
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
OR14569
Sigma Aldrich
14999
Matrix Scientific
041868
Academic Data
PubChem
7010034
Names and Identifiers
Synonyms
Boc-3-methyl-D-phenylalanine
3-Methyl-D-phenylalanine, N-BOC protected
Boc-D-3-甲基苯丙氨酸
Boc-D-Phe(3-Me)-OH
Boc-3-methyl-D-phenylalanine
IUPAC Traditional name
(2R)-2-[(tert-butoxycarbonyl)amino]-3-(3-methylphenyl)propanoic acid
IUPAC name
(2R)-2-{[(tert-butoxy)carbonyl]amino}-3-(3-methylphenyl)propanoic acid
Registration numbers
PubChem SID
24848995
161002276
MDL Number
MFCD01862943
CAS Number
114873-14-2
PubChem CID
7010034
Molecule Details
Sigma Aldrich
14999
Packaging
5 g in poly bottle
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Safety Information
MSDS Link
Download link
Source
Download link
Source
TSCA Listed
false
Source
Storage Warning
IRRITANT
Source
Irritant
Source
3
Source
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
Product Information
C15H21NO4
Source
≥98.0% (TLC)
Source
German water hazard class
Personal Protective Equipment
Empirical Formula (Hill Notation)
Purity