03768
′L-β-Homoproline′ hydrochloride
≥98.0% (TLC)
Synonym(s):
(S)-2-(2-Pyrrolidinyl)acetic acid hydrochloride
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Empirical Formula (Hill Notation):
C6H11NO2 · HCl
CAS Number:
Molecular Weight:
165.62
UNSPSC Code:
12352200
NACRES:
NA.26
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
471672
InChI
1S/C6H11NO2.ClH/c8-6(9)4-5-2-1-3-7-5;/h5,7H,1-4H2,(H,8,9);1H/t5-;/m0./s1
SMILES string
Cl.OC(=O)C[C@@H]1CCCN1
InChI key
VQDACVOAOJQTPR-JEDNCBNOSA-N
assay
≥98.0% (TLC)
form
powder
color
white to light brown
application(s)
peptide synthesis
Quality Level
Application
L-β-homoproline is a non-coded α-imino acid used in organic peptide synthesis.
Biochem/physiol Actions
L-β-Homoproline is a β amino acid useful in peptide and protein conformation studies.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
New bradykinin B(2) receptor antagonists - influence of C-terminal segment modifications on their pharmacological properties.
Sleszynska M, Kwiatkowska A, et al.
Acta Biochimica Polonica, 56, 6410648-6410648 (2009)
Dariusz Sobolewski et al.
Journal of peptide science : an official publication of the European Peptide Society, 15(3), 161-165 (2008-11-28)
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),D-Arg(8)]VP (dVDAVP) with L- or D-Pip, a non-coded
Sándor Góbi et al.
Physical chemistry chemical physics : PCCP, 12(41), 13603-13615 (2010-09-21)
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 landscape was investigated by infrared (IR) and vibrational circular dichroism (VCD) spectroscopy combined with density functional calculations. Based upon a comparison
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service