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Molecule
ID:38703
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₂₃H₁₉NO₄
Molecular Mass
373.40126
Exact Mass
373.13140809
Charge
0
InChI
InChI=1S/C23H19NO4/c25-22(26)21(15-8-2-1-3-9-15)24-23(27)28-14-20-18-12-6-4-10-16(18)17-11-5-7-13-19(17)20/h1-13,20-21H,14H2,(H,24,27)(H,25,26)/t21-/m0/s1
InChIKey
PCJHOCNJLMFYCV-NRFANRHFSA-N
Canonic Smiles
O=C(N[C@@H](c1ccccc1)C(=O)O)OCC1c2ccccc2c2c1cccc2
Isomeric Smiles
c1cccc(c1)[C@@H](C(=O)O)NC(=O)OCC1c2c(c3c1cccc3)cccc2
Calculated Properties
JChem
Acid pKa
3.7060661
H Acceptors
3
H Donor
2
LogD (pH = 5.5)
2.620036
LogD (pH = 7.4)
1.1099627
Log P
4.4129825
Molar Refractivity
104.4411
Polarizability
41.751896
Polar Surface Area
75.63
Rotatable Bonds
6
Lipinski's Rule of Five
true
Data Source
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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
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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
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Academic Data
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IUPAC name
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IUPAC Traditional name
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Synonyms
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Physical Property
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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
Academic Data
PubChem
7269367
Commercial Catalog
Sigma Aldrich
47531
Bide Pharmatech
BD17312
Matrix Scientific
041593
Names and Identifiers
IUPAC name
(2S)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-2-phenylacetic acid
IUPAC Traditional name
(S)-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}(phenyl)acetic acid
Synonyms
Fmoc-L-phenylglycine
Fmoc-L-α-苯基甘氨酸
Fmoc-Phg-OH
Fmoc-L-α-phenylglycine
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-phenylacetic acid
Registration numbers
CAS Number
102410-65-1
MDL Number
MFCD00155632
PubChem SID
161002010
24871109
PubChem CID
7269367
Beilstein Number
5309005
Molecule Details
Sigma Aldrich
47531
Packaging
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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PubChem CID
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Beilstein Number
Properties
Safety Information
MSDS Link
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Source
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Source
Storage Warning
IRRITANT
Source
TSCA Listed
false
Source
German water hazard class
3
Source
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
2-8°C
Source
Physical Property
[α]20/D +81±3°, c = 1% in DMF
Source
Product Information
C23H19NO4
Source
≥98.0% (HPLC)
Source
95+%
Source
Personal Protective Equipment
Storage Temperature
Optical Rotation
Empirical Formula (Hill Notation)
Purity