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Molecule
ID:38390
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₈H₁₅NO₄
Molecular Mass
189.209
Exact Mass
189.10010797
Charge
0
InChI
InChI=1S/C8H15NO4/c1-5(6(10)11)9-7(12)13-8(2,3)4/h5H,1-4H3,(H,9,12)(H,10,11)/t5-/m1/s1
InChIKey
QVHJQCGUWFKTSE-RXMQYKEDSA-N
Canonic Smiles
C[C@H](C(=O)O)NC(=O)OC(C)(C)C
Isomeric Smiles
C[C@H](C(=O)O)NC(=O)OC(C)(C)C
Calculated Properties
JChem
Acid pKa
3.9908156
H Acceptors
3
H Donor
2
LogD (pH = 5.5)
-0.6049154
LogD (pH = 7.4)
-2.2509282
Log P
0.91338605
Molar Refractivity
45.3703
Polarizability
17.99616
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
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Synonyms
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IUPAC name
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IUPAC Traditional name
Registration numbers
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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
MP Biomedicals
02199054
Sigma Aldrich
B0512
15048
Matrix Scientific
041260
Enamine
EN300-55380
Bide Pharmatech
BD8511
Alfa Aesar
B22706
Academic Data
PubChem
637606
Names and Identifiers
Synonyms
N-Alpha-t-Boc-D-alanine
Boc-D-alanine
Boc-D-Alanine
Boc-D-丙氨酸
Boc-D-Ala-OH
Boc-D-Ala-OH
N-(tert-Butoxycarbonyl)-D-alanine
N-Boc-D-丙氨酸
N-a-t-BOC-D-ALANINE
N-Boc-D-alanine
(2R)-2-{[(tert-butoxy)carbonyl]amino}propanoic acid
IUPAC name
(2R)-2-{[(tert-butoxy)carbonyl]amino}propanoic acid
IUPAC Traditional name
(2R)-2-[(tert-butoxycarbonyl)amino]propanoic acid
Registration numbers
CAS Number
7764-95-6
Beilstein Number
2048396
4905241
MDL Number
MFCD00063123
PubChem SID
24849036
161001697
PubChem CID
637606
Molecule Details
Sigma Aldrich
15048
Packaging
5, 25 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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Beilstein Number
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MDL Number
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PubChem SID
•
PubChem CID
Properties
Safety Information
Storage Warning
IRRITANT
Source
MSDS Link
Download link
Source
Download link
Source
Download link
Source
TSCA Listed
false
Source
否
Source
-20°C
Source
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
3
Source
Product Information
95%
Source
≥98.0% (TLC)
Source
98%
Source
98+%
Source
Download link
Source
CH3CH[NHCO2C(CH3)3]CO2H
Source
Physical Property
82 - 85°C
Source
81-84°C
Source
1.172
Source
+26 (c=2 in acetic acid)
Source
Storage Temperature
Personal Protective Equipment
German water hazard class
Purity
Certificate of Analysis
Linear Formula
Melting Point
Hydrophobicity(logP)
Optical Rotation