58202-80-5

Basic information

• Product Name: 2-<(S)-1-benzyloxycarbonylaminoethyl>-4-carbomethoxy-(R)-Δ2-thiazoline
• Synonyms: 2-<(S)-1-benzyloxycarbonylaminoethyl>-4-carbomethoxy-(R)-Δ2-thiazoline
• CAS NO: 58202-80-5
• Molecular Weight: 322.385
• Mol File: 58202-80-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-<(S)-1-benzyloxycarbonylaminoethyl>-4-carbomethoxy-(R)-Δ2-thiazoline(CAS DataBase Reference)
• NIST Chemistry Reference: 2-<(S)-1-benzyloxycarbonylaminoethyl>-4-carbomethoxy-(R)-Δ2-thiazoline(58202-80-5)
• EPA Substance Registry System: 2-<(S)-1-benzyloxycarbonylaminoethyl>-4-carbomethoxy-(R)-Δ2-thiazoline(58202-80-5)

Safety Data

• Hazardous Substances Data: 58202-80-5(Hazardous Substances Data)

Upstream product

• 34804-98-3 N-benzyloxycarbonyl-L-alanyl-L-cysteine methyl ester 
• 13139-29-2 2-benzyloxycarbonylamino-(S)-propioimino ethyl ether 
• 18598-63-5 L-cysteine methyl ester hydrochloride 

Downstream Products

• 132402-45-0 (S)-1-((S)-2-{[2-((S)-1-Benzyloxycarbonylamino-ethyl)-thiazole-4-carbonyl]-amino}-3-phenyl-propionyl)-pyrrolidine-2-carboxylic acid benzyl ester 
• 132402-44-9 (S)-1-((S)-2-{[2-((S)-1-Benzyloxycarbonylamino-ethyl)-thiazole-4-carbonyl]-amino}-3-phenyl-propionyl)-pyrrolidine-2-carboxylic acid tert-butyl ester 
• 68353-28-6 2-<(S)-1-benzyloxycarbonylaminoethyl>-4-carboxy-thiazole 
• 132402-42-7 2-<(S)-1-benzyloxycarbonylaminoethyl>-4-methoxycarbonylthiazole 

Relevant articles and documents

Catalytic synthesis of peptide-derived thiazolines and oxazolines using bis(quinolinolato)dioxomolybdenum(VI) complexes

Bis(2-ethyl-8-quinolinolato)dioxomolybdenum(VI) (9) (1 mol %) shows remarkable catalytic activity for the dehydrative cyclization of cysteine-containing dipeptides 1 to give the corresponding thiazolines 2 with less than 6 % epimerization at the C2-exomet

Molybdenum oxides as highly effective dehydrative cyclization catalysts for the synthesis of oxazolines and thiazolines

(Chemical Equation Presented) In the presence of molybdenum oxide the dehydrative cyclization of N-acylserines, N-acylthreonines, and N-acylcysteines can be carried out under Dean-Stark conditions in toluene to give oxazolines and thiazolines. The ammoniu