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Molecule
ID:66522
Structure
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Functional Group
Text
General Information
Structure
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Molecular Formula
C₉H₁₇NO₃
Molecular Mass
187.23618
Exact Mass
187.12084341
Charge
0
InChI
InChI=1S/C9H17NO3/c1-9(2,3)13-8(12)10-5-4-7(11)6-10/h7,11H,4-6H2,1-3H3/t7-/m0/s1
InChIKey
APCBTRDHCDOPNY-ZETCQYMHSA-N
Canonic Smiles
O[C@H]1CCN(C1)C(=O)OC(C)(C)C
Isomeric Smiles
N1(C[C@H](CC1)O)C(=O)OC(C)(C)C
Calculated Properties
JChem
Acid pKa
14.823066
H Acceptors
2
H Donor
1
LogD (pH = 5.5)
0.34841445
LogD (pH = 7.4)
0.34841442
Log P
0.34841445
Molar Refractivity
48.5474
Polarizability
19.142935
Polar Surface Area
49.77
Rotatable Bonds
2
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
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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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Synonyms
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IUPAC Traditional name
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IUPAC name
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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
Matrix Scientific
071932
Apollo Scientific
OR15680
Adesis
1-100
Sigma Aldrich
634786
06842
Enamine
EN300-77160
Bide Pharmatech
BD7089
Alfa Aesar
L19691
Academic Data
PubChem
854055
Names and Identifiers
Synonyms
(S)-(+)-N-Boc-3-pyrrolidinol
tert-Butyl (3S)-3-hydroxypyrrolidine-1-carboxylate
(3S)-1-(tert-Butoxycarbonyl)-3-hydroxypyrrolidine
(3S)-3-Hydroxypyrrolidine, N-BOC protected
(R)-3-Hydroxy-pyrrolidine-1-carboxylic acid tert-butyl ester
(S)-1-N-叔丁氧羰基-3-羟基吡咯烷
(S)-1-Boc-3-hydroxypyrrolidine
(S)-1-Boc-3-pyrrolidinol
(S)-1-Boc-3-羟基吡咯烷
tert-butyl (3S)-3-hydroxypyrrolidine-1-carboxylate
(S)-N-(tert-Butoxycarbonyl)-(+)-3-pyrrolidinol
(S)-N-(叔丁氧羰基)-(+)-3-吡咯烷醇
(S)-(+)-N-Boc-3-pyrrolidinol
(S)-(+)-1-Boc-3-hydroxypyrrolidine
(S)-(+)-1-Boc-3-羟基吡咯烷
(S)-(+)-1-tert-Butoxycarbonyl-3-hydroxypyrrolidine
(S)-(+)-1-Boc-3-pyrrolidinol
IUPAC Traditional name
tert-butyl (3S)-3-hydroxypyrrolidine-1-carboxylate
IUPAC name
tert-butyl (3S)-3-hydroxypyrrolidine-1-carboxylate
Registration numbers
MDL Number
MFCD01317839
CAS Number
101469-92-5
103057-44-9
PubChem CID
854055
PubChem SID
162032260
24882649
24845975
Beilstein Number
6271108
Molecule Details
Sigma Aldrich
634786
Application
Used in synthesis of ligands for the nicotinic acetylcholine receptor.1
Packaging
1, 5 g in glass bottle
References
PubChem Literature
From Data Sources
•
Product of Toray Industries, Inc.
Bioactivity
PubChem BioAssay
Registration numbers
•
MDL Number
•
CAS Number
•
PubChem CID
•
PubChem SID
•
Beilstein Number
Properties
•
Safety Information
•
Product Information
•
Physical Property
Properties
Safety Information
Storage Warning
IRRITANT
Source
Harmful/Irritant
Source
MSDS Link
Download link
Source
Download link
Source
Download link
Source
false
Source
否
Source
Acute toxicity (oral, dermal, inhalation), categories 1,2,3
Toxic (T)
P261
-
P280
-
P301+P310
-
P305+P351+P338
Source
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
UN 2811 6.1/PG 3
Source
26
-
39
-
45
Source
26
-
37
Source
Danger
Source
H301
-
H315
-
H318
-
H335
Source
H315
-
H319
-
H335
Source
2811
Source
25
-
37/38
-
41
Source
36/37/38
Source
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
Source
3
Source
3
Source
6.1
Source
Product Information
95+%
Source
97%
Source
≥98.0% (GC)
Source
95%
Source
98%
Source
99%, ee 99%
Source
C9H17NO3
Source
Physical Property
62-65°C
Source
60-64 °C(lit.)
Source
57-59 °C
Source
60 - 62°C
Source
62-65°C
Source
[α]20/D +26°, c = 1% in methanol
Source
[α]/D +26±1° in ethanol
Source
Source
Corrosive to metals, category 1
Skin corrosion, categories 1A,1B,1C
Serious eye damage, category 1
Source
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
Source
Irritant (Xi)
Source
Source
purum
Source
+28 (c=1 in methanol)
Source
Hydrophobicity(logP)
1.048
Source
TSCA Listed
GHS Pictograms
European Hazard Symbols
GHS Precautionary statements
RID/ADR
Safety Statements
GHS Signal Word
GHS Hazard statements
UN Number
Risk Statements
Personal Protective Equipment
Packing Group
German water hazard class
Hazard Class
Purity
Empirical Formula (Hill Notation)
Grade
Melting Point
Optical Rotation