56879-46-0,MFCD08458431
Catalog No.:AA00EEBX

56879-46-0 | 2-(Pyrrolidin-2-yl)acetic acid

Pack Size
Purity
Availability
Price(USD)
Quantity
  
100mg
95%
in stock  
$137.00   $96.00
- +
250mg
95%
in stock  
$195.00   $137.00
- +
1g
95%
in stock  
$444.00   $311.00
- +
5g
95%
in stock  
$1,316.00   $921.00
- +
10g
95%
in stock  
$2,182.00 $1,527.00
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA00EEBX
Chemical Name:
2-(Pyrrolidin-2-yl)acetic acid
CAS Number:
56879-46-0
Molecular Formula:
C6H11NO2
Molecular Weight:
129.1570
MDL Number:
MFCD08458431
SMILES:
OC(=O)CC1CCCN1
Properties
Properties
 
MP:
>115ºC (dec.)  
Storage:
Keep in dry area;2-8℃;  

Computed Properties
 
Complexity:
114  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0  
Rotatable Bond Count:
2  
Undefined Atom Stereocenter Count:
1  
Undefined Bond Stereocenter Count:
0  
XLogP3:
-2.4  

Literature

Title: Mechanism and optimisation of the homoboroproline bifunctional catalytic asymmetric aldol reaction: Lewis acid tuning through in situ esterification.

Journal: Organic & biomolecular chemistry 20120328

Title: Ruthenium-catalysed synthesis of fluorinated bicyclic amino esters through tandem carbene addition/cyclopropanation of enynes.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany) 20110816

Title: Is β-homo-proline a pseudo-γ-turn forming element of β-peptides? An IR and VCD spectroscopic study on Ac-β-HPro-NHMe in cryogenic matrices and solutions.

Journal: Physical chemistry chemical physics : PCCP 20101107

Title: Synthesis of alpha-cyclopropyl-beta-homoprolines.

Journal: The Journal of organic chemistry 20090605

Title: Improved protocol for asymmetric, intramolecular heteroatom Michael addition using organocatalysis: enantioselective syntheses of homoproline, pelletierine, and homopipecolic acid.

Journal: The Journal of organic chemistry 20080704

Title: Three-component synthesis of polysubstituted homoproline analogs.

Journal: Molecules (Basel, Switzerland) 20050831

Title: Synthesis and biological evaluation of new GABA-uptake inhibitors derived from proline and from pyrrolidine-2-acetic acid.

Journal: European journal of medicinal chemistry 20050301

Title: GABA uptake inhibitors. Design, molecular pharmacology and therapeutic aspects.

Journal: Current pharmaceutical design 20000801

Title: 1-(3-(9H-carbazol-9-yl)-1-propyl)-4-(2-methoxyphenyl)-4-piperidinol, a novel subtype selective inhibitor of the mouse type II GABA-transporter.

Journal: British journal of pharmacology 19970301

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SDS
Tags:56879-46-0 Molecular Formula|56879-46-0 MDL|56879-46-0 SMILES|56879-46-0 2-(Pyrrolidin-2-yl)acetic acid
Catalog No.: AA00EEBX
56879-46-0,MFCD08458431
56879-46-0 | 2-(Pyrrolidin-2-yl)acetic acid
Pack Size: 100mg
Purity: 95%
in stock
$137.00 $96.00
Pack Size: 250mg
Purity: 95%
in stock
$195.00 $137.00
Pack Size: 1g
Purity: 95%
in stock
$444.00 $311.00
Pack Size: 5g
Purity: 95%
in stock
$1,316.00 $921.00
Pack Size: 10g
Purity: 95%
in stock
$2,182.00 $1,527.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA00EEBX
Chemical Name: 2-(Pyrrolidin-2-yl)acetic acid
CAS Number: 56879-46-0
Molecular Formula: C6H11NO2
Molecular Weight: 129.1570
MDL Number: MFCD08458431
SMILES: OC(=O)CC1CCCN1
Properties
MP: >115ºC (dec.)  
Storage: Keep in dry area;2-8℃;  
Complexity: 114  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 9  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 2  
Isotope Atom Count: 0  
Rotatable Bond Count: 2  
Undefined Atom Stereocenter Count: 1  
Undefined Bond Stereocenter Count: 0  
XLogP3: -2.4  
Literature fold

Title: Mechanism and optimisation of the homoboroproline bifunctional catalytic asymmetric aldol reaction: Lewis acid tuning through in situ esterification.

Journal: Organic & biomolecular chemistry20120328

Title: Ruthenium-catalysed synthesis of fluorinated bicyclic amino esters through tandem carbene addition/cyclopropanation of enynes.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany)20110816

Title: Is β-homo-proline a pseudo-γ-turn forming element of β-peptides? An IR and VCD spectroscopic study on Ac-β-HPro-NHMe in cryogenic matrices and solutions.

Journal: Physical chemistry chemical physics : PCCP20101107

Title: Synthesis of alpha-cyclopropyl-beta-homoprolines.

Journal: The Journal of organic chemistry20090605

Title: Improved protocol for asymmetric, intramolecular heteroatom Michael addition using organocatalysis: enantioselective syntheses of homoproline, pelletierine, and homopipecolic acid.

Journal: The Journal of organic chemistry20080704

Title: Three-component synthesis of polysubstituted homoproline analogs.

Journal: Molecules (Basel, Switzerland)20050831

Title: Synthesis and biological evaluation of new GABA-uptake inhibitors derived from proline and from pyrrolidine-2-acetic acid.

Journal: European journal of medicinal chemistry20050301

Title: GABA uptake inhibitors. Design, molecular pharmacology and therapeutic aspects.

Journal: Current pharmaceutical design20000801

Title: 1-(3-(9H-carbazol-9-yl)-1-propyl)-4-(2-methoxyphenyl)-4-piperidinol, a novel subtype selective inhibitor of the mouse type II GABA-transporter.

Journal: British journal of pharmacology19970301

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