103310-88-9

Basic information

• Product Name: L-Isoleucine, phenylmethyl ester, hydrochloride
• CAS NO: 103310-88-9
• Molecular Formula: C13H19NO2.ClH
• Molecular Weight: 257.76
• Mol File: 103310-88-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: L-Isoleucine, phenylmethyl ester, hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: L-Isoleucine, phenylmethyl ester, hydrochloride(103310-88-9)
• EPA Substance Registry System: L-Isoleucine, phenylmethyl ester, hydrochloride(103310-88-9)

Safety Data

• Hazardous Substances Data: 103310-88-9(Hazardous Substances Data)

Upstream product

• 73-32-5 L-isoleucine 
• 100-51-6 benzyl alcohol 
• 100-44-7 benzyl chloride 

Downstream Products

• 62056-96-6 C₂₅H₂₈NO₃P 
• 103725-76-4 Boc-L-Pro-L-Ile-OBz 
• 42406-72-4 L-isoleucine benzyl ester 
• 731779-65-0 Boc-Δ(3)Pro-Ile-OBzl 
• 1177450-72-4 C₂₀H₂₅ClNO₅P 
• 122900-39-4 Sodium; {(S)-3-(4-amino-phenyl)-2-[(2S,3S)-2-(ethoxy-hydroxy-phosphorylamino)-3-methyl-pentanoylamino]-propionylamino}-acetate 
• 122900-11-2 N-(diethylphosphoryl)-L-isoleucyl-O-<<(N,N-dibenzylamino)carbonyl>methyl>-L-tyrosylglycine methyl ester 
• 122900-07-6 N-(diethylphosphoryl)-L-isoleucyl-O-<<(N-benzylamino)carbonyl>methyl>-L-tyrosylglycine methyl ester 
• 122900-04-3 N-(diethylphosphoryl)-L-isoleucyl-O-<(benzyloxycarbonyl)methyl>-L-tyrosylglycine methyl ester 
• 122900-01-0 N-(diethylphosphoryl)-L-isoleucyl-O-(tetrahydro-2-pyranyl)-L-tyrosylglycine ethyl ester 
• 122900-16-7 N-(diethylphosphoryl)-L-isoleucyl-4-nitro-L-phenylalanylglycine methyl ester 
• 122900-15-6 N-(diethylphosphoryl)-L-isoleucyl-4-amino-L-phenylalanylglycine methyl ester 
• 122899-92-7 {(S)-2-[(2S,3S)-2-(Diethoxy-phosphorylamino)-3-methyl-pentanoylamino]-propionylamino}-acetic acid benzyl ester 
• 93627-78-2 C₁₈H₂₂NO₃P*C₁₂H₂₃N 

Relevant articles and documents

Esterification of unprotected a-Amino acids in ionic liquids as the reaction media

Ionic liquid 1,3-dimethylimidazolium methanesulfonate was used to prepare a-amino acids benzylic esters from unprotected amino acids and benzyl chloride. Esterification of several amino acids was achieved with satisfactory yields: by-products can be removed by a simple work-up procedure to afford the pure product. The described method is simple, mild, rapid and save.

Study on synthesis, characteristics and catalysis properties of novel chiral metal complexes catalysts for 1,3-dipolar cycloaddition reactions of nitrone with electron-rich alkene

As a new class of potential catalysts for 1,3-dipolar cycloaddition reactions, fourteen L-amino acid Schiff base Cu(II) and Ti(IV) complexes were synthesized, characterized, and evaluated for their catalytic activities in the reaction between C, N-diphenylnitrone and electron-rich ethyl vinyl ether under both homogeneous and in situ conditions. The methods for preparation and utilization of the catalysts were elucidated in detail, and the results of the catalytic reactions were described and discussed as well. Excellent reaction results were found in the presence of some catalysts (20 mol%) with > 90% endo-isoazolidines produced, compared with predominantly exo-isoazolidine produced without a catalyst. In addition, the reaction rate is found to be enhanced remarkably by a Cu(II) complex Schiff base catalyst at room temperature.