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Molecule
ID:38661
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₂₄H₂₇NO₄
Molecular Mass
393.47548
Exact Mass
393.19400835
Charge
0
InChI
InChI=1S/C24H27NO4/c26-23(27)22(14-16-8-2-1-3-9-16)25-24(28)29-15-21-19-12-6-4-10-17(19)18-11-5-7-13-20(18)21/h4-7,10-13,16,21-22H,1-3,8-9,14-15H2,(H,25,28)(H,26,27)/t22-/m0/s1
InChIKey
HIJAUEZBPWTKIV-QFIPXVFZSA-N
Canonic Smiles
O=C(N[C@H](C(=O)O)CC1CCCCC1)OCC1c2ccccc2c2c1cccc2
Isomeric Smiles
[C@H](CC1CCCCC1)(C(=O)O)NC(=O)OCC1c2c(c3c1cccc3)cccc2
Calculated Properties
JChem
Acid pKa
3.9593003
H Acceptors
3
H Donor
2
LogD (pH = 5.5)
3.6208134
LogD (pH = 7.4)
1.9874604
Log P
5.1694074
Molar Refractivity
110.2515
Polarizability
44.319756
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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Academic Data
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Commercial Catalog
Names and Identifiers
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Synonyms
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IUPAC Traditional name
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IUPAC name
Registration numbers
Properties
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Safety Information
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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
•
PubChem BioAssay
Data Source
Academic Data
PubChem
978326
Commercial Catalog
Sigma Aldrich
47314
Matrix Scientific
041550
Names and Identifiers
Synonyms
Fmoc-3-cyclohexyl-L-alanine
Fmoc-Cha-OH
Fmoc-beta-cyclohexyl-L-alanine
N-芴甲氧羰基-3-环己基-L-丙氨酸
IUPAC Traditional name
(2S)-3-cyclohexyl-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}propanoic acid
IUPAC name
(2S)-3-cyclohexyl-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}propanoic acid
Registration numbers
MDL Number
MFCD00065614
PubChem SID
24870875
161001968
Beilstein Number
7052264
CAS Number
135673-97-1
PubChem CID
978326
Molecule Details
Sigma Aldrich
47314
Packaging
1 g in poly bottle
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay
Registration numbers
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MDL Number
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PubChem SID
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Beilstein Number
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CAS Number
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PubChem CID
Properties
Safety Information
MSDS Link
Download link
Source
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Source
TSCA Listed
false
Source
Storage Warning
IRRITANT
Source
Storage Temperature
2-8°C
Source
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
3
Source
Product Information
C24H27NO4
Source
≥98.0% (TLC)
Source
Personal Protective Equipment
German water hazard class
Empirical Formula (Hill Notation)
Purity