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40499-83-0,MFCD00005256
Catalog No.:AA0033PF

40499-83-0 | Pyrrolidin-3-ol

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
97%
in stock  
$18.00   $13.00
- +
5g
97%
in stock  
$23.00   $16.00
- +
10g
97%
in stock  
$41.00   $29.00
- +
25g
97%
in stock  
$89.00   $62.00
- +
100g
97%
in stock  
$349.00   $245.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA0033PF
Chemical Name:
Pyrrolidin-3-ol
CAS Number:
40499-83-0
Molecular Formula:
C4H9NO
Molecular Weight:
87.1204
MDL Number:
MFCD00005256
SMILES:
OC1CNCC1
NSC Number:
89294
Properties
Properties
 
BP:
224.7±0.0°C at 760 mmHg  
Form:
Liquid  
Refractive Index:
n20/D 1.49(lit.)  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
46.8  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
6  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Undefined Atom Stereocenter Count:
1  
XLogP3:
-0.7  

Literature

Title: Monosubstituted γ-lactam and conformationally constrained 1,3-diaminopropan-2-ol transition-state isostere inhibitors of β-secretase (BACE).

Journal: Bioorganic & medicinal chemistry letters 20111115

Title: A 4-hydroxypyrrolidine-catalyzed mannich reaction of aldehydes: control of anti-selectivity by hydrogen bonding assisted by Brønsted acids.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany) 20100510

Title: Synthesis and chiroptical properties of chiral azoaromatic dendrimers with a C3-symmetrical core.

Journal: Chirality 20100101

Title: Discovery of orally available integrin alpha5beta1 antagonists.

Journal: Bioorganic & medicinal chemistry letters 20100101

Title: Samarium diiodide promoted generation and asymmetric hydroxyalkylation of N,O-diprotected (3S)-3-pyrrolidinol 2-carbanions.

Journal: Organic letters 20050217

Title: Preparation of (R)- and (S)-N-protected 3-hydroxypyrrolidines by hydroxylation with Sphingomonas sp. HXN-200, a highly active, regio- and stereoselective, and easy to handle biocatalyst.

Journal: The Journal of organic chemistry 20011214

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SDS
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