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Molecule
ID:103048
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₀H₁₁NO₃
Molecular Mass
193.19924
Exact Mass
193.07389322
Charge
0
InChI
InChI=1S/C10H11NO3/c1-7(10(13)14)11-9(12)8-5-3-2-4-6-8/h2-7H,1H3,(H,11,12)(H,13,14)/t7-/m0/s1
InChIKey
UAQVHNZEONHPQG-ZETCQYMHSA-N
Canonic Smiles
C[C@@H](C(=O)O)NC(=O)c1ccccc1
Isomeric Smiles
C[C@H](NC(=O)c1ccccc1)C(=O)O
Calculated Properties
JChem
Acid pKa
3.6599452
H Acceptors
3
H Donor
2
LogD (pH = 5.5)
-0.74319506
LogD (pH = 7.4)
-2.2268627
Log P
1.0943097
Molar Refractivity
50.6116
Polarizability
19.234276
Polar Surface Area
66.4
Rotatable Bonds
3
Lipinski's Rule of Five
true
Data Source
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Related Proteins
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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
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RDKit
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Synonyms
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IUPAC name
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IUPAC Traditional name
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Related Proteins
Molecular Spectra
Molecule Details
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MP Biomedicals
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PubChem Literature
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
MP Biomedicals
02150443
Sigma Aldrich
B3750
Academic Data
PubChem
709778
Names and Identifiers
Synonyms
N-α-BENZOYL-L-ALANINE
Bz-Ala-OH
N-Benzoyl-L-alanine
IUPAC name
(2S)-2-(phenylformamido)propanoic acid
IUPAC Traditional name
(2S)-2-(phenylformamido)propanoic acid
Registration numbers
CAS Number
2198-64-3
EC Number
218-601-3
PubChem SID
24891732
162090180
MDL Number
MFCD00063128
PubChem CID
709778
Molecule Details
MP Biomedicals
02150443
Crystalline
References
PubChem Literature
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Bioactivity
PubChem BioAssay
Registration numbers
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CAS Number
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EC Number
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PubChem SID
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MDL Number
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PubChem CID
Properties
Product Information
Certificate of Analysis
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Source
Safety Information
Storage Condition
0°C
Source
MSDS Link
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Source
Storage Temperature
-20°C
Source
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
3
Source
Personal Protective Equipment
German water hazard class