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Molecule
ID:39083
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₂₄H₂₀INO₄
Molecular Mass
513.32437
Exact Mass
513.04370613
Charge
0
InChI
InChI=1S/C24H20INO4/c25-16-11-9-15(10-12-16)13-22(23(27)28)26-24(29)30-14-21-19-7-3-1-5-17(19)18-6-2-4-8-20(18)21/h1-12,21-22H,13-14H2,(H,26,29)(H,27,28)/t22-/m0/s1
InChIKey
LXOXXTQKKRJNNB-QFIPXVFZSA-N
Canonic Smiles
O=C(N[C@H](C(=O)O)Cc1ccc(cc1)I)OCC1c2ccccc2c2c1cccc2
Isomeric Smiles
c1(ccc(cc1)C[C@@H](C(=O)O)NC(=O)OCC1c2c(c3c1cccc3)cccc2)I
Calculated Properties
JChem
Acid pKa
3.167656
H Acceptors
3
H Donor
2
LogD (pH = 5.5)
3.3229718
LogD (pH = 7.4)
2.1796272
Log P
5.630588
Molar Refractivity
122.5586
Polarizability
48.57136
Polar Surface Area
75.63
Rotatable Bonds
7
Lipinski's Rule of Five
false
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
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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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Synonyms
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IUPAC Traditional name
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IUPAC name
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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
OR14612
Sigma Aldrich
468746
47431
Alfa Aesar
H51977
Matrix Scientific
041984
Academic Data
PubChem
2761479
Names and Identifiers
Synonyms
4-Iodo-L-phenylalanine, N-FMOC protected
Fmoc-4-iodo-L-phenylalanine
Fmoc-Phe(4-I)-OH
Fmoc-Phe(4-I)-OH
Fmoc-4-碘-L-苯丙氨酸
Fmoc-4-iodo-L-phenylalanine
N-芴甲氧羰基-L-4-碘苯丙氨酸
Fmoc-L-4-碘苯丙氨酸
N-(9-Fluorenylmethoxycarbonyl)-3-(4-iodophenyl)-L-alanine
Fmoc-(4-iodo)-Phe-OH
N-Fmoc-4-碘-L-苯基丙氨酸
N-Fmoc-4-iodo-L-phenylalanine
IUPAC Traditional name
(2S)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-3-(4-iodophenyl)propanoic acid
IUPAC name
(2S)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-3-(4-iodophenyl)propanoic acid
Registration numbers
MDL Number
MFCD00672340
CAS Number
82565-68-2
PubChem SID
24870532
161002390
24870986
PubChem CID
2761479
Beilstein Number
4592723
Molecule Details
Sigma Aldrich
47431
Other Notes
Synthesis of a phosphotyrosine mimetic1; Building block employed for the synthesis of peptides carrying a radio-label2
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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MDL Number
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CAS Number
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PubChem SID
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PubChem CID
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Beilstein Number
Properties
Safety Information
MSDS Link
Download link
Source
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Storage Warning
IRRITANT
Source
Irritant
Source
Light Sensitive
Source
false
Source
否
Source
3
Source
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
2-8°C
Source
Product Information
97%
Source
≥97.0%
Source
95%
Source
C24H20INO4
Source
Physical Property
[α]22/D -10°, c = 1 in DMF
Source
-10 (c=1 in DMF)
Source
213-217 °C(lit.)
Source
213-217°C
Source
TSCA Listed
German water hazard class
Personal Protective Equipment
Storage Temperature
Purity
Empirical Formula (Hill Notation)
Optical Rotation
Melting Point