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Molecule
ID:38936
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₄H₁₈ClNO₄
Molecular Mass
299.75002
Exact Mass
299.09243574
Charge
0
InChI
InChI=1S/C14H18ClNO4/c1-14(2,3)20-13(19)16-11(12(17)18)8-9-6-4-5-7-10(9)15/h4-7,11H,8H2,1-3H3,(H,16,19)(H,17,18)/t11-/m0/s1
InChIKey
TUUQJNHCVFJMPU-NSHDSACASA-N
Canonic Smiles
O=C(OC(C)(C)C)N[C@H](C(=O)O)Cc1ccccc1Cl
Isomeric Smiles
c1cc(c(cc1)C[C@@H](C(=O)O)NC(=O)OC(C)(C)C)Cl
Calculated Properties
JChem
Acid pKa
3.8244765
H Acceptors
3
H Donor
2
LogD (pH = 5.5)
1.4951982
LogD (pH = 7.4)
-0.07721409
Log P
3.173757
Molar Refractivity
74.7941
Polarizability
29.416647
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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IUPAC Traditional name
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IUPAC name
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Synonyms
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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
OR14541
Sigma Aldrich
15021
Matrix Scientific
041833
Academic Data
PubChem
2761463
Names and Identifiers
IUPAC Traditional name
(2S)-2-[(tert-butoxycarbonyl)amino]-3-(2-chlorophenyl)propanoic acid
IUPAC name
(2S)-2-{[(tert-butoxy)carbonyl]amino}-3-(2-chlorophenyl)propanoic acid
Synonyms
2-Chloro-D-phenylalanine, N-BOC protected
Boc-2-chloro-L-phenylalanine
Boc-Phe(2-Cl)-OH
Boc-2-chloro-L-phenylalanine
Boc-L-2-氯苯丙氨酸
Registration numbers
CAS Number
114873-02-8
80102-23-4
MDL Number
MFCD00672514
MFCD00801056
PubChem SID
161002243
24848847
Beilstein Number
8778440
PubChem CID
2761463
Properties
Safety Information
TSCA Listed
false
来源
MSDS Link
Download link
Source
Download link
Source
Storage Warning
IRRITANT
Source
Irritant
Source
German water hazard class
3
Source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
Product Information
Purity
≥98.0% (TLC)
Source
Empirical Formula (Hill Notation)
C14H18ClNO4
Source
Physical Property
Melting Point
94-100 °C
Source
Optical Rotation
[α]20/D -24.5±1°, c = 1% in ethyl acetate
Source
Molecule Details
Sigma Aldrich
15021
Packaging
1 g in poly tube
5 g in poly bottle
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Registration numbers
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CAS Number
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MDL Number
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PubChem SID
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Beilstein Number
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PubChem CID