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Molecule
ID:88264
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/c1-15(2,3)20-14(19)16-10-12(13(17)18)9-11-7-5-4-6-8-11/h4-8,12H,9-10H2,1-3H3,(H,16,19)(H,17,18)/t12-/m1/s1
InChIKey
ZYCITKXROAFBAR-GFCCVEGCSA-N
Canonic Smiles
OC(=O)[C@H](Cc1ccccc1)CNC(=O)OC(C)(C)C
Isomeric Smiles
O=C([C@@H](CNC(=O)OC(C)(C)C)Cc1ccccc1)O
Calculated Properties
JChem
Acid pKa
4.5233073
H Acceptors
3
H Donor
2
LogD (pH = 5.5)
1.6839514
LogD (pH = 7.4)
-0.087045945
Log P
2.7029934
Molar Refractivity
74.8463
Polarizability
29.333641
Polar Surface Area
75.63
Rotatable Bonds
7
Lipinski's Rule of Five
true
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Molecular Spectra
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Molecule Details
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Bioactivity
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IUPAC name
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From Data Sources
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Data Source
Commercial Catalog
Apollo Scientific
OR40214
Sigma Aldrich
698660
Bide Pharmatech
BD32942
A&J Pharmtech
AJA-O28078
Academic Data
PubChem
7176387
Names and Identifiers
Synonyms
(2R)-2-Benzyl-3-[(tert-butoxycarbonyl)amino]propanoic acid
(2R)-2-(tert-Butoxycarbonylamino)methyl-3-phenylpropanoic acid
(R)-2-Benzyl-3-(tert-butoxycarbonylamino)propanoic acid
(R)-2-苄基-3-(Boc-氨基)丙酸
(R)-2-[(Boc-amino)methyl]-3-phenylpropionic acid
(R)-2-[(Boc-氨基)甲基]-3-苯基丙酸
(R)-2-Benzyl-3-(Boc-amino)propionic acid
(R)-2-Benzyl-Boc-β-alanine
(R)-2-苄基-Boc-β-丙氨酸
IUPAC Traditional name
(2R)-2-benzyl-3-[(tert-butoxycarbonyl)amino]propanoic acid
IUPAC name
(2R)-2-benzyl-3-{[(tert-butoxy)carbonyl]amino}propanoic acid
Registration numbers
MDL Number
MFCD07372496
CAS Number
262301-38-2
PubChem CID
7176387
PubChem SID
162104574
Properties
Safety Information
Storage Warning
Irritant
Source
European Hazard Symbols
Irritant (Xi)
Source
Risk Statements
43
Source
GHS Signal Word
Warning
Source
Safety Statements
36/37
Source
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
Source
GHS Hazard statements
H317
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Source
German water hazard class
3
Source
MSDS Link
Download link
Source
GHS Precautionary statements
P280
Source
Physical Property
Optical Rotation
[α]22/D +15.0°, c = 1 in chloroform
Source
Melting Point
94-102 °C
Source
Product Information
Purity
97%
Source
95+%
Source
98%
Source
Empirical Formula (Hill Notation)
C15H21NO4
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay