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Molecule
ID:39171
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₅H₂₁NO₅
Molecular Mass
295.33094
Exact Mass
295.14197278
Charge
0
InChI
InChI=1S/C15H21NO5/c1-15(2,3)21-14(19)16-12(13(17)18)10-20-9-11-7-5-4-6-8-11/h4-8,12H,9-10H2,1-3H3,(H,16,19)(H,17,18)/t12-/m0/s1
InChIKey
DMBKPDOAQVGTST-LBPRGKRZSA-N
Canonic Smiles
OC(=O)[C@@H](NC(=O)OC(C)(C)C)COCc1ccccc1
Isomeric Smiles
[C@H](COCc1ccccc1)(C(=O)O)NC(=O)OC(C)(C)C
Calculated Properties
JChem
Acid pKa
3.9243522
H Acceptors
4
H Donor
2
LogD (pH = 5.5)
0.65184385
LogD (pH = 7.4)
-0.9667642
Log P
2.2340758
Molar Refractivity
76.2778
Polarizability
30.053162
Polar Surface Area
84.86
Rotatable Bonds
8
Lipinski's Rule of Five
true
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Related Proteins
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Molecular Spectra
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Molecule Details
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General Information
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MP Biomedicals
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
MP Biomedicals
02150486
Sigma Aldrich
15390
Bide Pharmatech
BD8532
Matrix Scientific
042076
Academic Data
PubChem
90234
Names and Identifiers
IUPAC Traditional name
(2S)-3-(benzyloxy)-2-[(tert-butoxycarbonyl)amino]propanoic acid
Synonyms
Boc-L-Ser(OBzl)-OH
Boc-Ser(Bzl)-OH
N-(tert-Butoxycarbonyl)-O-benzyl-L-serine
N-α-t-BOC-O-BENZYL-L-SERINE
N-Boc-O-Benzyl-L-serine
Boc-O-苄基-L-丝氨酸
Boc-Ser(Bzl)-OH
N-(叔丁氧羰基)-O-苄基-L-丝氨酸
Boc-O-benzyl-L-serine
IUPAC name
(2S)-3-(benzyloxy)-2-{[(tert-butoxy)carbonyl]amino}propanoic acid
Registration numbers
MDL Number
MFCD00066063
CAS Number
23680-31-1
PubChem SID
161002478
24849386
PubChem CID
90234
Beilstein Number
3064461
EC Number
245-820-1
Properties
Safety Information
MSDS Link
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Source
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Source
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TSCA Listed
false
Source
Storage Warning
IRRITANT
Source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
German water hazard class
3
Source
Product Information
Certificate of Analysis
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Source
Linear Formula
C6H5CH2OCH2CH(COOH)NHCOOC(CH3)3
Source
Purity
≥99.0% (T)
Source
95+%
Source
Physical Property
Optical Rotation
[α]20/D +20±1°, c = 2% in ethanol: water (4:1)
Source
Melting Point
58-60 °C(lit.)
Source
Molecule Details
MP Biomedicals
02150486
Crystalline
Sigma Aldrich
15390
Packaging
5, 25 g in poly bottle
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PubChem Literature
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Bioactivity
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