ChemicalBook Product Catalog Biochemical Engineering Amino Acids and Derivatives Proline derivatives L-Proline benzyl ester hydrochloride

L-Proline benzyl ester hydrochloride

L-Proline benzyl ester hydrochloride Basic information
Product Name:L-Proline benzyl ester hydrochloride
Synonyms:L-PYRROLIDINE-2-CARBOXYLIC ACID BENZYL ESTER HCL;L-PROLINE BENZYL ESTER;L-PROLINE BENZYL ESTER HCL;L-PROLINE BENZYL ESTER HYDROCHLORIDE SALT;L-PROLINE BENZYL ESTER MONOHYDROCHLORIDE;H-PRO-OBZL;H-PRO-OBZL HCL;PROLINE-OBZL HCL
CAS:16652-71-4
MF:C12H16ClNO2
MW:241.71
EINECS:240-700-5
Product Categories:Proline [Pro, P];Amino Acids and Derivatives;Amino Acid Benzyl Esters;Amino Acids (C-Protected);Biochemistry;Amino hydrochloride;Amino Acid Derivatives;Peptide Synthesis;Proline;Amino Acids;Amino Acid Derivatives
Mol File:16652-71-4.mol
L-Proline benzyl ester hydrochloride Structure
L-Proline benzyl ester hydrochloride Chemical Properties
Melting point 148-151 °C(lit.)
alpha -44 º (c=1, methanol)
refractive index 1.4365
storage temp. Inert atmosphere,Room Temperature
solubility soluble in Methanol
form Crystalline Powder
color White to pale yellow
optical activity[α]20/D 48°, c = 1 in H2O
Water Solubility miscible
Sensitive Hygroscopic
BRN 3598081
InChIKeyNEDMOHHWRPHBAL-MERQFXBCSA-N
CAS DataBase Reference16652-71-4(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 36/38-36/37/38-22
Safety Statements 22-24/25-37/39-26-36/37/39
WGK Germany 3
HS Code 29339900
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
ALFA English
L-Proline benzyl ester hydrochloride Usage And Synthesis
Chemical PropertiesWhite powder
UsesL-Proline Benzyl Ester Hydrochloride acts as a reagent in the synthesis and bioactivity of a goralatide analog with anti-leukemic activity.
L-Proline benzyl ester hydrochloride Preparation Products And Raw materials
Raw materials1,2-Pyrrolidinedicarboxylic acid, 1-(1,1-dimethylethyl) 2-(phenylmethyl) ester, (2S)--->L-Proline-->BOC-L-Proline-->Benzyl alcohol
BOC-L-TRANSPRO(4-CN)-OBN (S,S)-2-Azabicyclo[3,3,0]-octane-3-carboxylic acid benzylester hydrochloride BENZYL-N-BOC-L-PYROGLUTAMATE BOC-L-TRANSPRO(OTS)-OBN Z-PYROGLUTAMYL PROLINE BENZYL ESTER L-4-HYDROXY-PROLINE BENZYL ESTER HYDROCHLORIDE,L-4-HYDROXY-PROLINE BENZYL ESTER HYDROCH,TRANS-4-HYDROXY-L-PROLINE BENZYL ESTER HCL Topotecan hydrochloride (2S,4R)-4-HYDROXY-PROLINE BENZYL ESTER, TOLUENE SULFONIC ACID SALT (2S,4R)-BENZYL-BOC-GAMMA-(4-BROMOBENZYL)-PYROGLUTAMATE (2S,4R)-BENZYL-BOC-GAMMA-BENZYLPYROGLUTAMATE (1S,3S,5S)-2-Azabicyclo[3,3,0]octane-3-carborylic acid benzyl ester hydrochloride BOC-HYP-OBZL FMOC-PRO-2-CL-TRT RESIN BOC-L-PRO-O-CH2-PHI-CH2-COOH H-PRO-P-NITROBENZYL ESTER HBR Benzyl formate Benzyl (2S,3aR,7aS)-octahydroindole-2-carboxylate hydrochloride Benzyl
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