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Molecule
ID:38990
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/c1-10-5-7-11(8-6-10)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
JYRWNPUFECDJCX-GFCCVEGCSA-N
Canonic Smiles
O=C(OC(C)(C)C)N[C@@H](C(=O)O)Cc1ccc(cc1)C
Isomeric Smiles
c1(ccc(cc1)C[C@H](C(=O)O)NC(=O)OC(C)(C)C)C
Calculated Properties
JChem
Acid pKa
4.136744
H Acceptors
3
H Donor
2
LogD (pH = 5.5)
1.7044097
LogD (pH = 7.4)
0.007651149
Log P
3.083134
Molar Refractivity
75.0305
Polarizability
29.258196
Polar Surface Area
75.63
Rotatable Bonds
6
Lipinski's Rule of Five
true
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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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Data Source
Commercial Catalog
Apollo Scientific
OR14573
Sigma Aldrich
15003
Matrix Scientific
041889
Academic Data
PubChem
7006640
Names and Identifiers
IUPAC Traditional name
(2R)-2-[(tert-butoxycarbonyl)amino]-3-(4-methylphenyl)propanoic acid
Synonyms
4-Methyl-D-phenylalanine, N-BOC protected
Boc-4-methyl-D-phenylalanine
Boc-D-4-甲基苯丙氨酸
Boc-D-Phe(4-Me)-OH
Boc-4-methyl-D-phenylalanine
IUPAC name
(2R)-2-{[(tert-butoxy)carbonyl]amino}-3-(4-methylphenyl)propanoic acid
Registration numbers
MDL Number
MFCD01317726
CAS Number
80102-27-8
PubChem SID
24849001
161002297
PubChem CID
7006640
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Safety Information
MSDS Link
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Source
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Source
Storage Warning
IRRITANT
Source
Irritant
Source
TSCA Listed
false
Source
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
3
Source
Product Information
≥98.0% (TLC)
Source
C15H21NO4
Source
Physical Property
84-88 °C
Source
[α]20/D -16±2°, c = 1% in methanol
Source
Personal Protective Equipment
German water hazard class
Purity
Empirical Formula (Hill Notation)
Melting Point
Optical Rotation