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104641-60-3 molecular structure
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(3R)-1-methylpyrrolidin-3-ol

ChemBase ID: 63306
Molecular Formular: C5H11NO
Molecular Mass: 101.14694
Monoisotopic Mass: 101.08406398
SMILES and InChIs

SMILES:
[C@@H]1(CN(C)CC1)O
Canonical SMILES:
CN1CC[C@H](C1)O
InChI:
InChI=1S/C5H11NO/c1-6-3-2-5(7)4-6/h5,7H,2-4H2,1H3/t5-/m1/s1
InChIKey:
FLVFPAIGVBQGET-RXMQYKEDSA-N

Cite this record

CBID:63306 http://www.chembase.cn/molecule-63306.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
(3R)-1-methylpyrrolidin-3-ol
IUPAC Traditional name
(3R)-1-methylpyrrolidin-3-ol
Synonyms
(R)-1-Methylpyrrolidin-3-ol
(R)-3-Hydroxy-1-methylpyrrolidine
(R)-(-)-1-Methyl-3-pyrrolidinol
(R)-(-)-1-Methyl-3-hydroxypyrrolidine
(3R)-1-Methylpyrrolidin-3-ol
(R)-N-Methyl-3-pyrrolidinol
(R)-(-)-3-Hydroxy-N-methylpyrrolidine
(R)-(-)-1-Methyl-3-pyrrolidinol
(R)-3-Hydroxy-1-methyl-pyrrolidine
(R)-(-)-1-甲基-3-羟基吡咯烷
(R)-(-)-3-羟基-N-甲基吡咯烷
(R)-(-)-1-甲基-3-吡咯烷醇
CAS Number
104641-60-3
104641-59-0
EC Number
000-000-0
MDL Number
MFCD03788747
Beilstein Number
4349393
PubChem SID
24883519
162029045
PubChem CID
6951332

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 14.847978  H Acceptors
H Donor LogD (pH = 5.5) -3.8714778 
LogD (pH = 7.4) -2.432706  Log P -0.5517307 
Molar Refractivity 28.847 cm3 Polarizability 11.356206 Å3
Polar Surface Area 23.47 Å2 Rotatable Bonds
Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Physical Property Safety Information Product Information Bioassay(PubChem)
Boiling Point
103-106°C/35mm expand Show data source
50-52 °C/1 mmHg(lit.) expand Show data source
Flash Point
158 °F expand Show data source
70 °C expand Show data source
70°C(158°F) expand Show data source
Density
0.920 expand Show data source
0.921 g/mL at 25 °C(lit.) expand Show data source
Refractive Index
1.4640 expand Show data source
n20/D 1.4640(lit.) expand Show data source
Optical Rotation
[α]20/D -7°, c = 1% in chloroform expand Show data source
Storage Warning
Air Sensitive & Hygroscopic expand Show data source
IRRITANT expand Show data source
European Hazard Symbols
Irritant Irritant (Xi) expand Show data source
MSDS Link
Download expand Show data source
Download expand Show data source
German water hazard class
3 expand Show data source
Risk Statements
36/37/38 expand Show data source
36/38 expand Show data source
Safety Statements
23-26-37 expand Show data source
26-36 expand Show data source
TSCA Listed
false expand Show data source
expand Show data source
GHS Pictograms
GHS07 expand Show data source
GHS Signal Word
Warning expand Show data source
GHS Hazard statements
H315-H319-H227 expand Show data source
H315-H319-H335 expand Show data source
GHS Precautionary statements
P210-P305+P351+P338-P302+P352-P321-P403+P235-P501A expand Show data source
P261-P305 + P351 + P338 expand Show data source
Personal Protective Equipment
Eyeshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter expand Show data source
Purity
>95% expand Show data source
97% expand Show data source
98% expand Show data source
99%, ee 99% expand Show data source
Empirical Formula (Hill Notation)
C5H11NO expand Show data source

DETAILS

DETAILS

Sigma Aldrich Sigma Aldrich
Sigma Aldrich - 647241 external link
Packaging
1, 5 g in glass bottle
Application
Reactant for:
• Asymmetric synthesis of constrained (-)-S-adenosyl-L-homocysteine (SAH) analogs as DNA methyltransferase inhibitors1
• Preparation of diaryl acylaminopyrimidines as adenosine A2A antagonists2
• Synthesis of analogs of istaroxime, a potent inhibitor of Na+,K+-ATPase3
• Synthesis of pharmacologically active stereoisomers of N-substituted soft anticholinergics4

REFERENCES

REFERENCES

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PATENTS

PATENTS

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INTERNET

INTERNET

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