N-Boc-trans-4-Hydroxy-L-proline methyl ester
N-Boc-trans-4-Hydroxy-L-proline methyl ester
  • CAS No.:74844-91-0
Other grades of this product :
N-Boc-trans-4-Hydroxy-L-proline methyl ester Basic information
Product Name:N-Boc-trans-4-Hydroxy-L-proline methyl ester
Synonyms:N-T-BOC-TRANS-4-HYDROXY-L-PROLINE METHYL ESTER;N-(TERT-BUTOXYCARBONYL)-TRANS-HYDROXYL-L-PROLINE METHYL ESTER;N-ALPHA-T-BUTOXYCARBONYL-L-HYDROXYPROLINE METHYL ESTER;N-BOC-TRANS-4-HYDROXYL-L-PROLINE METHYL ESTER;N-BOC-TRANS-4-HYDROXY-L-PROLINE METHYL ESTER;N-BOC-4-HYDROXY-L-PROLINE METHYL ESTER;N-BOC-L-TRANS-4-HYDROXY-PROLINE METHYL ESTER;(2R,4R)-4-HYDROXY-PYRROLIDINE-1,2-DICARBOXYLIC ACID 1-TERT-BUTYL ESTER 2-METHYL ESTER
CAS:74844-91-0
MF:C11H19NO5
MW:245.27
EINECS:616-143-2
Product Categories:Amino Acids and Derivatives;Hydroxyproline [Hyp];Unusual Amino Acids;Amino Acids 13C, 2H, 15N;Boc-Amino acid series;Amino Acids & Derivatives;Heterocycles;Peptide Synthesis;Proline Derivatives;Unnatural Amino Acid Derivatives;1
Mol File:74844-91-0.mol
N-Boc-trans-4-Hydroxy-L-proline methyl ester Chemical Properties
Melting point 92-96 °C (lit.)
alpha -65 º (c=1 CHCl3)
Boiling point 132°C/0.05mmHg(lit.)
density 1.216±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility Soluble in chloroform, dichloromethane and ethyl acetate.
form Crystalline Powder
pka14.27±0.40(Predicted)
color White to light beige
optical activity[α]20/D -65°, c = 1% in chloroform
InChIKeyMZMNEDXVUJLQAF-SFYZADRCSA-N
LogP0.813 at 25℃
CAS DataBase Reference74844-91-0(CAS DataBase Reference)
Safety Information
Hazard Codes Xn
Risk Statements 20/21/22-36/37/38
Safety Statements 24/25-36-26
WGK Germany 3
HazardClass IRRITANT
HS Code 29339900
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
N-Boc-trans-4-Hydroxy-L-proline methyl ester Usage And Synthesis
Chemical PropertiesClear Colourless Oil
UsesA potential iNOS inhibitor.
Uses(2S,4R)-4-Hydroxypyrrolidine-1,2-dicarboxylic Acid 1-tert-Butyl Ester 2-Methyl Ester roline scaffold.
UsesIt is used in the synthesis of For-Met-Leu-Phe-OMe (fMLF-OMe) analogues based on Met residue replacement by 4-amino-proline scaffold.

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