93967-75-0

Basic information

• Product Name: N-BOC-METHYL(2S,4S)-4-PHENOXY-2-PYRROLIDINECARBOXYLATE
• Synonyms: N-BOC-METHYL(2S,4S)-4-PHENOXY-2-PYRROLIDINECARBOXYLATE;Methyl (2S,4S)-N-Boc-4-phenoxy-2-pyrrolidinecarboxylate
• CAS NO: 93967-75-0
• Molecular Formula: C₁₇H₂₃NO₅
• Molecular Weight: 321.37
• Mol File: 93967-75-0.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-BOC-METHYL(2S,4S)-4-PHENOXY-2-PYRROLIDINECARBOXYLATE(CAS DataBase Reference)
• NIST Chemistry Reference: N-BOC-METHYL(2S,4S)-4-PHENOXY-2-PYRROLIDINECARBOXYLATE(93967-75-0)
• EPA Substance Registry System: N-BOC-METHYL(2S,4S)-4-PHENOXY-2-PYRROLIDINECARBOXYLATE(93967-75-0)

Safety Data

• Hazardous Substances Data: 93967-75-0(Hazardous Substances Data)

Usage

General Description

N-BOC-METHYL(2S,4S)-4-PHENOXY-2-PYRROLIDINECARBOXYLATE is a chemical compound that belongs to the class of pyrrolidinecarboxylic acid derivatives. It is a white solid substance used in the synthesis of various pharmaceutical and agrochemical products. N-BOC-METHYL(2S,4S)-4-PHENOXY-2-PYRROLIDINECARBOXYLATE is a derivative of pyrrolidine, which is a five-membered heterocyclic compound containing a nitrogen atom. The presence of the phenoxy group in its structure suggests potential applications in the development of new drugs targeting specific biological pathways. Additionally, the BOC (tert-butoxycarbonyl) protecting group attached to the nitrogen atom plays a crucial role in the synthesis and modification of various chemical compounds. Overall, N-BOC-METHYL(2S,4S)-4-PHENOXY-2-PYRROLIDINECARBOXYLATE is a versatile chemical intermediate with potential uses in the pharmaceutical industry.

Upstream product

• 13726-69-7 (2S,4R)-4-hydroxy-1-[(2-methylpropan-2-yl)oxycarbonyl]pyrrolidine-2-carboxylic acid 
• 74844-91-0 (2S,4S)-N-tert-butoxycarbonyl-4-hydroxyproline methyl ester 
• 108-95-2 phenol 
• 74844-91-0 1-tert-butyl 2-methyl (2S,4R)-4-hydroxy-1,2-pyrrolidinedicarboxylate 

Downstream Products

• 317357-19-0 (2S,4S)-tert-butyl 2-(hydroxymethyl)-4-phenoxypyrrolidine-1-carboxylate 
• 886447-49-0 ethyl [4-[1-[3-methoxy-4-[N'-(2-methylphenyl)ureido]phenylacetyl]-(4S)-phenoxy-(2S)-pyrrolidinylcarbonyl]-1-piperazinyl]acetate 
• 886447-83-2 ethyl [4-[1-tert-butoxycarbonyl-(4S)-phenoxy-(2S)-pyrrolidinylcarbonyl]-1-piperazinyl]acetate 
• 886447-39-8 [4-((2S,4S)-4-Phenoxy-pyrrolidine-2-carbonyl)-piperazin-1-yl]-acetic acid ethyl ester 
• 147266-79-3 (2S,4S)-1-(tert-butoxycarbonyl)-4-phenoxypyrrolidine-2-carboxylic acid 
• 157187-62-7 (2S,4S)-4-Phenoxy-pyrrolidine-2-carboxylic acid methyl ester 

Relevant articles and documents

SMAC MIMETICS USED AS IAP INHIBITORS AND USE THEREOF

Disclosed are a class of SMAC mimetics used as IAP inhibitors, and in particular disclosed are compounds as shown in formula (I), isomers thereof, and pharmaceutically acceptable salts thereof. The IAP inhibitors are drugs for treating cancers, in particu

VLA-4 INHIBITORS

The present invention relates to a compound represented by the following formula (I): (wherein, W represents WA-A1 -WB - (in which, WA is substituted or unsubstituted aryl, etc., A1 is -NR1-, single bond, -C(O)-, etc., and WB is substituted or unsubstituted arylene, etc.), R is single bond, -NH-, -OCH2-, alkenylene, etc., X is -C(O) -CH2-, etc., and M is, for example, the following formula: (in which, R11, R12 and R13 each independently represents hydrogen, hydroxyl, amino, halogen, etc., R14 is hydrogen or lower alkyl, Y represents -CH2-O-, etc., Z is substituted or unsubstituted arylene, etc., A2 is single bond, etc, and R10 is hydroxyl or lower alkoxy)), or salt thereof; and a medicament containing the same. This compound or salt thereof selectively inhibits binding of cell adhesion molecules to VAL-4 and exhibits high bioavailability so that it is useful as a preventive and/or remedy for inflammatory diseases, autoimmune diseases, metastasis, bronchial asthma, rhinostenosis, diabetes, and the like.