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Molecule
ID:69473
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₀H₁₉NO₃
Molecular Mass
201.26276
Exact Mass
201.13649347
Charge
0
InChI
InChI=1S/C10H19NO3/c1-10(2,3)14-9(13)11-6-4-5-8(11)7-12/h8,12H,4-7H2,1-3H3/t8-/m1/s1
InChIKey
BFFLLBPMZCIGRM-MRVPVSSYSA-N
Canonic Smiles
OC[C@H]1CCCN1C(=O)OC(C)(C)C
Isomeric Smiles
N1([C@H](CCC1)CO)C(=O)OC(C)(C)C
Calculated Properties
JChem
Acid pKa
15.09024
H Acceptors
2
H Donor
1
LogD (pH = 5.5)
0.86577713
LogD (pH = 7.4)
0.8657771
Log P
0.86577713
Molar Refractivity
53.192
Polarizability
20.97339
Polar Surface Area
49.77
Rotatable Bonds
3
Lipinski's Rule of Five
true
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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
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IUPAC Traditional name
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IUPAC name
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Sigma Aldrich
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
OR14516
Shanghai Lingjing
127
Sigma Aldrich
469440
15522
Matrix Scientific
074959
Academic Data
PubChem
688279
Names and Identifiers
Synonyms
tert-Butyl (2S)-(+)-2-(hydroxymethyl)pyrrolidine-1-carboxylate
(2S)-(+)-1-(tert-Butoxycarbonyl)-2-(hydroxymethyl)pyrrolidine
(2S)-(+)-2-(Hydroxymethyl)pyrrolidine, N-BOC protected
(R)-tert-Butyl 2-(hydroxymethyl)-pyrrolidine-1-carboxylate
Boc-D-脯氨醇
N-t-Boc-D-prolinol
Boc-D-Prolinol
(R)-(+)-1-Boc-2-pyrrolidinemethanol
N-Boc-D-脯氨醇
(R)-(+)-1-(tert-Butoxycarbonyl)-2-pyrrolidinemethanol
(R)-(+)-1-(叔丁氧羰基)-2-吡咯烷甲醇
N-叔丁氧羰基-D-脯氨醇
N-Boc-D-prolinol
(R)-1-Boc-2-pyrrolidinemethanol
N-Boc-D-prolinol
(R)-1-叔丁氧羰基-2-吡咯烷甲醇
IUPAC Traditional name
tert-butyl (2R)-2-(hydroxymethyl)pyrrolidine-1-carboxylate
IUPAC name
tert-butyl (2R)-2-(hydroxymethyl)pyrrolidine-1-carboxylate
Registration numbers
CAS Number
83435-58-9
69610-40-8
MDL Number
MFCD00040580
MFCD00066232
PubChem SID
24849497
24870602
162035199
Beilstein Number
3650011
PubChem CID
688279
Properties
Product Information
Purity
95+%
Source
98%
Source
≥99.0% (TLC)
Source
Empirical Formula (Hill Notation)
C10H19NO3
Source
Grade
puriss.
Source
Safety Information
TSCA Listed
false
Source
Storage Warning
IRRITANT
Source
Irritant/Keep Cold
Source
MSDS Link
Download link
Source
Download link
Source
Download link
Source
Risk Statements
36/37/38
Source
German water hazard class
3
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
GHS Signal Word
Warning
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
GHS Precautionary statements
P261
-
P305+P351+P338
Source
European Hazard Symbols
Irritant (Xi)
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
Safety Statements
26
-
36
Source
Physical Property
Melting Point
62-64°C
Source
59-62°C
Source
60-64 °C(lit.)
Source
59-62 °C
Source
Boiling Point
150°C/4mm
Source
Solubility
不溶于水
Source
Optical Rotation
49°(589nm, C=1.3, CHCl3)
Source
[α]23/D +50°, c = 1.3 in chloroform
Source
[α]20/D +54±2°, c = 5% in methanol
Source
Molecule Details
Sigma Aldrich
469440
Packaging
1 g in glass 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