Basic information Uses Safety Supplier Related

(S)-(+)-1-Methyl-3-pyrrolidinol

Basic information Uses Safety Supplier Related

(S)-(+)-1-Methyl-3-pyrrolidinol Basic information

Product Name:
(S)-(+)-1-Methyl-3-pyrrolidinol
Synonyms:
  • (S)-3-HYDROXY-1-METHYL-PYRROLIDINE
  • (R)-3-Hydroxy-1-methylpyr...
  • (S)-(+)-1-Methyl-3-pyrrolidinol, ee 99%, 98%
  • (S)-(+)-1-Methyl-3-pyrrolidinol, 98%, ee 99%
  • (3S)-1-methylpyrrolidin-3-ol
  • (S)-(+)-1-Methyl-3-pyrrolidinol 95%
  • (S)-N-Methyl-3-pyrrolidinol
  • (S)-N-Methyl-3-pyrrolidinol,99%e.e.
CAS:
104641-59-0
MF:
C5H11NO
MW:
101.15
EINECS:
677-547-2
Product Categories:
  • Chiral Building Blocks
  • Simple Alcohols (Chiral)
  • Pyrrole&Pyrrolidine&Pyrroline
  • Synthetic Organic Chemistry
Mol File:
104641-59-0.mol
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(S)-(+)-1-Methyl-3-pyrrolidinol Chemical Properties

Boiling point:
181-182 °C(lit.)
alpha 
6 º (c=1%, chloroform)
Density 
0.993 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.4660(lit.)
Flash point:
192 °F
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
form 
Liquid
pka
14.95±0.20(Predicted)
color 
Colorless to yellow to brown
optical activity
[α]20/D +6°, c = 1 in chloroform
Sensitive 
Air Sensitive & Hygroscopic
BRN 
4349394
CAS DataBase Reference
104641-59-0(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
RIDADR 
NA 1993 / PGIII
WGK Germany 
3
RTECS 
TM9570000
HS Code 
29339900

MSDS

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(S)-(+)-1-Methyl-3-pyrrolidinol Usage And Synthesis

Uses

(S)-1-Methyl-3-pyrrolidinol is a useful synthetic intermediate. It is used to prepare diaryl acylaminopyrimidines as adenosine A2A antagonists. It is also used to synthesize (alkoxyamino)(pyridinylamino)pyrazinecarbonitriles as selective checkpoint kinase 1 (CHK1) inhibitors with oral antitumor activities.

Uses

(S)-1-Methyl-3-pyrrolidinol is a useful synthetic intermediate. It is used to prepare diaryl acylaminopyrimidines as adenosine A2A antagonists. It is also used to synthesize (alkoxyamino)(pyridinylamino)pyrazinecarbonitriles as selective checkpoint kinase 1 (CHK1) inhibitors with oral antitumor activities.

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