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trans-4-Hydroxy-L-proline methyl ester hydrochloride

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CAS:40216-83-9
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CAS:40216-83-9
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CAS:40216-83-9
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Purity:98% HPLC Package:5MG;10MG;50MG;100MG,1G,5G

trans-4-Hydroxy-L-proline methyl ester hydrochloride manufacturers

  • H-L-Hyp-Ome·HCl
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  • $0.00 / 1kg
  • 2026-01-30
  • CAS:40216-83-9
  • Min. Order: 1kg
  • Purity: 98%
  • Supply Ability: 1T+
trans-4-Hydroxy-L-proline methyl ester hydrochloride Basic information
Product Name:trans-4-Hydroxy-L-proline methyl ester hydrochloride
Synonyms:H-HYP-OME HCL;H-L-HYP-OME HCL;HYDROXYPROLINE-OME HCL;(2S,4R)-trans-4-hydroxy-L-proline methyl ester hydrochloride;4-hydroxy-2-pyrrolidinecarboxylic acid methyl ester hydrochloride;L-4-HYDROXYPROLINE METHYL ESTER HYDROCHLORIDE;L-4-HYDROXYPROLINE METHYL ESTER HYDROCHLORIDE SALT;L-4-TRANS-HYDROXYPROLINE METHYL ESTER HYDROCHLORIDE
CAS:40216-83-9
MF:C6H12ClNO3
MW:181.62
EINECS:609-795-4
Product Categories:Peptide Synthesis;Proline Derivatives;Unnatural Amino Acid Derivatives;Amino Acids & Derivatives;Chiral Reagents;Heterocycles;Hydroxyproline [Hyp];Nitrogen cyclic compounds;Amino Acid Derivatives;Amino Acids
Mol File:40216-83-9.mol
trans-4-Hydroxy-L-proline methyl ester hydrochloride Structure
trans-4-Hydroxy-L-proline methyl ester hydrochloride Chemical Properties
Melting point 169 °C
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility DMSO (Slightly), Methanol (Slightly), Water (Slightly, Sonicated)
form Solid
color White to Off-White
BRN 4716932
Stability:Hygroscopic
Major Applicationpeptide synthesis
InChIInChI=1/C6H11NO3.ClH/c1-10-6(9)5-2-4(8)3-7-5;/h4-5,7-8H,2-3H2,1H3;1H/t4-,5+;/s3
InChIKeyKLGSHNXEUZOKHH-SRJSDOSHNA-N
SMILES[C@@H]1(NC[C@H](O)C1)C(=O)OC.Cl |&1:0,3,r|
CAS DataBase Reference40216-83-9(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Safety Statements 24/25
WGK Germany 3
HS Code 29339900
Storage Class11 - Combustible Solids
MSDS Information
trans-4-Hydroxy-L-proline methyl ester hydrochloride Usage And Synthesis
Chemical PropertiesWhite Solid
Usestrans-4-Hydroxy-L-proline (H952376) derivative. A natural constituent of animal structural proteins such as collagen and elastin.
reaction suitabilityreaction type: solution phase peptide synthesis
Synthesis
Methanol

67-56-1

Trans-4-Hydroxy-L-proline Hydrochloride

32968-78-8

trans-4-Hydroxy-L-proline methyl ester hydrochloride

40216-83-9

The general procedure for synthesizing trans-4-hydroxy-L-proline methyl ester hydrochloride from methanol and trans-4-hydroxy-L-proline hydrochloride is as follows: Example 1: (2S,4R)-4-hydroxy-2-pyrrolidine carboxylic acid hydrochloride (1.0 g, 7.6 mmol) was dissolved in methanol (25 mL) and cooled to 0°C. Thionyl chloride (0.83 mL, 11.4 mmol) was added slowly under stirring. The reaction mixture was gradually warmed to room temperature and subsequently heated to reflux overnight. After completion of the reaction, it was cooled to room temperature and the reaction mixture was concentrated to dryness under reduced pressure to afford trans-4-hydroxy-L-proline methyl ester hydrochloride (1.2 g, 92% yield) in white solid form. The structure of the product was confirmed by 1H NMR (300 MHz, DMSO-d6).

IC 50Non-cleavable Linker
References[1] Organic Letters, 2018, vol. 20, # 1, p. 162 - 165
[2] Patent: WO2013/174937, 2013, A1. Location in patent: Page/Page column 74
[3] Patent: US2015/152048, 2015, A1. Location in patent: Paragraph 0447-0448
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