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(2S)-2-(carboxymethyl)pyrrolidinium chloride

Names

[ CAS No. ]:
53912-85-9

[ Name ]:
(2S)-2-(carboxymethyl)pyrrolidinium chloride

[Synonym ]:
2-Pyrrolidineacetic acid, (2S)-, hydrochloride (1:1)
(2S)-2-(carboxymethyl)pyrrolidinium chloride
(2S)-2-Pyrrolidinylacetic acid hydrochloride (1:1)
MFCD07363484
(S)-2-(Pyrrolidin-2-yl)acetic acid hydrochloride
2-[(2S)-pyrrolidin-2-yl]acetic acid,hydrochloride
(S)-2-(2-Pyrrolidinyl)acetic acid hydrochloride

Chemical & Physical Properties

[ Melting Point ]:
208-210°C

[ Molecular Formula ]:
C6H12ClNO2

[ Molecular Weight ]:
165.618

[ Exact Mass ]:
165.055649

[ PSA ]:
49.33000

[ LogP ]:
1.34390

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi

[ Risk Phrases ]:
R36/37/38:Irritating to eyes, respiratory system and skin .

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

Articles

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.

Phys. Chem. Chem. Phys. 12 , 13603-13615, (2010)

In order to test the pseudo-γ-turn forming capability of β-homo-proline (β(3)-HPro) 2-[(2S)-1-acetylpyrrolidin-2-yl]-N-methylacetamide (Ac-β(3)-HPro-NHMe) was synthesized and its potential energy land...

Analogues of AVP modified in the N-terminal part of the molecule with Pip isomers: TFA-catalysed peptide bond hydrolysis.

J. Pept. Sci. 15 , 161-165, (2009)

Using SPPS techniques, six new analogues of AVP and some of its agonists were synthesised. The peptides were designed by substitution of Phe at position 3 of AVP, [Mpa(1)] AVP (dAVP) and [Mpa(1),Val(4...

New bradykinin B(2) receptor antagonists - influence of C-terminal segment modifications on their pharmacological properties. Sleszyńska M, Kwiatkowska A, et al.

Acta Biochim. Pol. 56 , 6410648, (2009)


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