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Molecule
ID:63248
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₉H₁₈N₂O₂
Molecular Mass
186.25142
Exact Mass
186.13682783
Charge
0
InChI
InChI=1S/C9H18N2O2/c1-9(2,3)13-8(12)11-5-4-7(10)6-11/h7H,4-6,10H2,1-3H3/t7-/m1/s1
InChIKey
CMIBWIAICVBURI-SSDOTTSWSA-N
Canonic Smiles
N[C@@H]1CCN(C1)C(=O)OC(C)(C)C
Isomeric Smiles
N1(C[C@H](N)CC1)C(=O)OC(C)(C)C
Calculated Properties
JChem
H Acceptors
2
H Donor
1
LogD (pH = 5.5)
-2.73314
LogD (pH = 7.4)
-1.7008487
Log P
0.24153264
Molar Refractivity
50.2049
Polarizability
20.017399
Polar Surface Area
55.56
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
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
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Names and Identifiers
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Synonyms
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IUPAC Traditional name
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IUPAC name
Registration numbers
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MDL Number
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PubChem SID
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CAS Number
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PubChem CID
Properties
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Product Information
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Safety 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
Apollo Scientific
OR4634
Matrix Scientific
068563
Sigma Aldrich
644064
Chemik
CHH16022
Enamine
EN300-89565
Bide Pharmatech
BD5526
Alfa Aesar
H28188
Academic Data
PubChem
854070
Names and Identifiers
Synonyms
tert-Butyl (3S)-3-aminopyrrolidine-1-carboxylate
(3S)-3-Amino-1-(tert-butoxycarbonyl)pyrolidine
(3S)-3-Aminopyrrolidine, N1-BOC protected
(R)-1-BOC-3-Aminopyrrolidine
tert-Butyl (3R)-3-aminopyrrolidine-1-carboxylate
(R)-(+)-N-Boc-3-氨基吡咯烷
(R)-(+)-1-Boc-3-氨基吡咯烷
tert-Butyl (R)-(+)-3-aminopyrrolidine-1-carboxylate
(R)-tert-Butyl 3-aminopyrrolidine-1-carboxylate
(R)-(+)-N-Boc-3-aminopyrrolidine
(R)-(+)-1-tert-Butoxycarbonyl-3-aminopyrrolidine
(R)-(+)-1-Boc-3-aminopyrrolidine
IUPAC Traditional name
tert-butyl (3R)-3-aminopyrrolidine-1-carboxylate
IUPAC name
tert-butyl (3R)-3-aminopyrrolidine-1-carboxylate
Registration numbers
MDL Number
MFCD03419272
MFCD03419271
PubChem SID
24883312
162028987
CAS Number
147081-49-0
147081-44-5
PubChem CID
854070
Molecule Details
Sigma Aldrich
644064
Packaging
1, 5 g in glass bottle
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay
Properties
Product Information
Purity
>95%
Source
97%
Source
95%
Source
Empirical Formula (Hill Notation)
C9H18N2O2
Source
Safety Information
TSCA Listed
false
Source
否
Source
MSDS Link
Download link
Source
Download link
Source
Storage Warning
IRRITANT
Source
Corrosive/Air Sensitive/Moisture Sensitive/Store under Argon
Source
Air Sensitive
Source
RID/ADR
UN 2810 6.1/PG 3
Source
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), categories 1,2,3
Source
Corrosive to metals, category 1
Skin corrosion, categories 1A,1B,1C
Serious eye damage, category 1
GHS Signal Word
Danger
Source
Hazard Class
6.1
Source
8
Source
GHS Hazard statements
H301
-
H318
Source
H314
-
H318
-
H227
Source
European Hazard Symbols
Harmful (Xn)
Source
Corrosive (C)
Risk Statements
22
-
41
-
44
Source
34
Source
UN Number
2810
Source
UN2735
Source
GHS Precautionary statements
P280
-
P301+P310
-
P305+P351+P338
Source
P210
-
P260
-
P303+P361+P353
-
P305+P351+P338
-
P405
-P501A
Source
Packing Group
3
Source
III
Source
German water hazard class
3
Source
Supplemental Hazard Statements
Risk of explosion if heated under confinement.
Source
Personal Protective Equipment
Eyeshields, Faceshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
Source
Safety Statements
26
-
36/37/39
Source
26
-
36/37/39
-
45
Source
Physical Property
Flash Point
91°C
Source
91 °C
Source
195.8 °F
Source
91°C(196°F)
Source
Boiling Point
216-217°C
Source
243-244 °C(lit.)
Source
243-244°C
Source
1.067
Source
1.098 g/mL at 25 °C(lit.)
Source
1.098
Source
1.4720
Source
n20/D 1.472(lit.)
Source
1.125
Source
+3.5 (c=1 in chloroform)
Source
Source
Source
Density
Refractive Index
Hydrophobicity(logP)
Optical Rotation