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Molecule
ID:38799
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₂H₁₅NO₄
Molecular Mass
237.2518
Exact Mass
237.10010797
Charge
0
InChI
InChI=1S/C12H15NO4/c1-12(2,3)17-11(16)13-9-6-4-8(5-7-9)10(14)15/h4-7H,1-3H3,(H,13,16)(H,14,15)
InChIKey
ZJDBQMWMDZEONW-UHFFFAOYSA-N
Canonic Smiles
O=C(Nc1ccc(cc1)C(=O)O)OC(C)(C)C
Isomeric Smiles
c1cc(ccc1NC(=O)OC(C)(C)C)C(=O)O
Calculated Properties
JChem
Acid pKa
4.1167707
H Acceptors
4
H Donor
2
LogD (pH = 5.5)
1.1440426
LogD (pH = 7.4)
-0.54653245
Log P
2.5417898
Molar Refractivity
63.6064
Polarizability
23.793444
Polar Surface Area
75.63
Rotatable Bonds
4
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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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
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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
Maybridge
SPB08182
Sigma Aldrich
15299
Alfa Aesar
L18531
Enamine
EN300-14053
Bide Pharmatech
BD14086
Matrix Scientific
041694
Academic Data
PubChem
2755931
Names and Identifiers
Synonyms
Boc-4-aminobenzoic acid
4-[(tert-butoxycarbonyl)amino]benzoic acid
4-(Boc-amino)benzoic acid
N-tert-Butoxycarbonyl-4-aminobenzoic acid
N-Boc-4-氨基苯甲酸
4-(Boc-amino)benzoic acid
Boc-4-Abz-OH
4-((tert-Butoxycarbonyl)amino)benzoic acid
4-(叔丁氧羰基氨基)苯甲酸
IUPAC Traditional name
4-[(tert-butoxycarbonyl)amino]benzoic acid
IUPAC name
4-{[(tert-butoxy)carbonyl]amino}benzoic acid
Registration numbers
CAS Number
66493-39-8
MDL Number
MFCD00037428
PubChem SID
24849274
161002106
Beilstein Number
2115614
PubChem CID
2755931
Properties
Safety Information
Storage Warning
IRRITANT
Source
TSCA Listed
false
Source
否
Source
MSDS Link
Download link
Source
Download link
Source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
German water hazard class
3
Source
GHS Precautionary statements
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
Source
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
Source
Risk Statements
36/37/38
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
Safety Statements
26
-
37
Source
European Hazard Symbols
Irritant (Xi)
Source
Product Information
Purity
97%
Source
≥98.0% (T)
Source
95%
Source
Linear Formula
(CH3)3CO2CNHC6H4CO2H
Source
Physical Property
Melting Point
~200 °C (dec.)
Source
193 - 195°C
Source
ca 193°C dec.
Source
Hydrophobicity(logP)
2.831
Source
Molecule Details
Sigma Aldrich
15299
Other Notes
BOC-protected derivative of PABA.1
Packaging
5, 50 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