113034-36-9

Basic information

• Product Name: ethyl (2E,4S)-4-<(benzyl)oxy>-2-pentenoate
• Synonyms: ethyl (2E,4S)-4-<(benzyl)oxy>-2-pentenoate
• CAS NO: 113034-36-9
• Molecular Weight: 234.295
• Mol File: 113034-36-9.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: ethyl (2E,4S)-4-<(benzyl)oxy>-2-pentenoate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl (2E,4S)-4-<(benzyl)oxy>-2-pentenoate(113034-36-9)
• EPA Substance Registry System: ethyl (2E,4S)-4-<(benzyl)oxy>-2-pentenoate(113034-36-9)

Safety Data

• Hazardous Substances Data: 113034-36-9(Hazardous Substances Data)

Upstream product

• 867-13-0 diethoxyphosphoryl-acetic acid ethyl ester 
• 81445-44-5 (S)-2-(benzyloxy)propanal 
• 1099-45-2 ethyl (triphenylphosphoranylidene)acetate 
• 54783-72-1 ethyl (S)-2-(benzyloxy)propionate 
• 136113-13-8 (S)-(2-benzyloxy)-1-nitropropane 
• 777931-82-5 (S)-4-Benzyloxy-2-hydroxy-3-nitro-pentanoic acid ethyl ester 
• 64-17-5 ethanol 
• 112489-57-3 (E)-(S)-[MeCH(OCH₂C₆H₅)CHCHCO₂Me] 

Downstream Products

• 124891-22-1 (E)-(S)-4-Benzyloxy-pent-2-enoic acid 
• 119242-59-0 (2E,4S)-4-<(benzyl)oxy>-2-pentenol 
• 116525-15-6 ethyl-2,3-dihydroxy-4-benzyloxypentanoate 
• 116490-97-2 ethyl-2,3-dihydroxy-4-benzyloxypentanoate 
• 116560-94-2 (2S)-(3R)-(4S)-5-deoxyxylono-1,4-lactone 
• 76647-70-6 (3R,4R,5S)-3,4-dihydroxy-5-methyldihydrofuran-2(3H)-one 
• 1025949-14-7 2,2,2-Trichloro-acetimidic acid (E)-(S)-4-benzyloxy-pent-2-enyl ester 
• 124988-79-0 <3S,3aS,6aS(S)>-Tetrahydro-3-(1-(phenylmethoxy)ethyl)-1-(phenylmethyl)-1H,6H-furo<3,4-c>isoxazol-6-one 
• 124891-02-7 (S)-(Nitrooxy)acetic acid 4-(phenylmethoxy)-(E)-pent-2-enyl ester 
• 124891-14-1 C₂₁H₂₃NO₄ 
• 124890-97-7 Bromo-acetic acid (E)-(S)-4-benzyloxy-pent-2-enyl ester 
• 124891-08-3 Oxo-acetic acid (E)-(S)-4-benzyloxy-pent-2-enyl ester 
• 124891-28-7 (S)-4-Benzyloxy-3-phenylsulfanyl-pentanoic acid allyl ester 
• 124891-25-4 (S)-(E)-4-(Phenylmethoxy)pent-2-enoic acid prop-2-enyl ester 

Relevant articles and documents

ENANTIOSELECTIVE SYNTHESIS OF γ-AMINO-α,β-UNSATURATED CARBOXYLIC ACID DERIVATIVES

Provided is an enantioselective, palladium-catalyzed method for the preparation of γ-amino-α,β-unsaturated carboxylic acid derivatives having the formulas II, III, IV and VIII.

Flexible and simple route for the stereoselective synthesis of trisubstituted γ-butyrolactones: Total synthesis of (+)-blastomycinone and its analogs

A flexible route for the stereoselective synthesis of trisubstituted γ-butyrolactones, namely (+)-blastomycinone and its analogs, is devised by the Sharpless asymmetric epoxidation and the regioselective ring opening reaction with dibutylcopper lithium as

Diastereoselective synthesis of enantiopure 5-[2-(alkoxyalkyl)-1- (hydroperoxypropyl)]-3-alkoxycarbonyl-2-alkyl furans

The diastereoselective approach to enantiomerically pure furyl hydroperoxides of general type 1 has been accomplished starting from (S)-(- )-ethyl lactate. In the first part of the synthesis the alkylating reagents 7a,b were efficiently produced to be use