146257-00-3

Basic information

• Product Name: 1-TERT-BUTYL 3-ETHYL 1H-PYRROLE-1,3(2H,5H)-DICARBOXYLATE
• Synonyms: 1-TERT-BUTYL 3-ETHYL 1H-PYRROLE-1,3(2H,5H)-DICARBOXYLATE;Ethyl N-Boc-2,5-dihydropyrrole-3-carboxylate;Ethyl N-tert-butoxycarbonyl-2,5-dihydropyrrole-3-carboxylate;1-O-tert-butyl 3-O-ethyl 2,5-dihydropyrrole-1,3-dicarboxylate
• CAS NO: 146257-00-3
• Molecular Formula: C₁₂H₁₉NO₄
• Molecular Weight: 241.285
• Mol File: 146257-00-3.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-TERT-BUTYL 3-ETHYL 1H-PYRROLE-1,3(2H,5H)-DICARBOXYLATE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-TERT-BUTYL 3-ETHYL 1H-PYRROLE-1,3(2H,5H)-DICARBOXYLATE(146257-00-3)
• EPA Substance Registry System: 1-TERT-BUTYL 3-ETHYL 1H-PYRROLE-1,3(2H,5H)-DICARBOXYLATE(146257-00-3)

Safety Data

• Hazardous Substances Data: 146257-00-3(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
1-TERT-BUTYL 3-ETHYL 1H-PYRROLE-1,3(2H,5H)-DICARBOXYLATE is used as a key building block for the synthesis of various drugs and pharmaceutical compounds. Its unique chemical structure contributes to the development of new medications, enhancing the therapeutic options available in the market.
Used in Chemical Industry:
In the chemical industry, 1-TERT-BUTYL 3-ETHYL 1H-PYRROLE-1,3(2H,5H)-DICARBOXYLATE serves as an important intermediate in the production of various chemical products. Its versatility in chemical reactions allows for the creation of a wide range of compounds with diverse applications.

Upstream product

• 146256-98-6 4-oxo-pyrrolidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-ethyl ester 
• 146256-99-7 tert-butyl 3-ethyl 4-hydroxypyrrolidine-1,3-dicarboxylate 

Downstream Products

• 2696257-44-8 C₂₁H₃₀N₂O₄ 
• 35516-95-1 ethyl 2,5-dihydro-1H-pyrrole-3-carboxylate 
• 72519-12-1 2,5-dihydro-1H-pyrrole-3-carboxylic acid 
• 267230-40-0 (3S,4R)-1-(N-tert-butoxycarbonyl)-3-[(1'R)-phenylethylamino]-4-ethoxycarbonylpyrrolidine 

Relevant articles and documents

Iridium-catalyzed enantioselective hydrogenation of unsaturated heterocyclic acids

Spiral binding: A highly enantioselective hydrogenation of unsaturated heterocyclic acids has been developed by using chiral iridium/spirophosphino oxazoline catalysts (see scheme; BArF-=tetrakis[3,5- bis(trifluoromethyl)phenyl]borate, Boc=tert-butoxycarbonyl). This reaction provided an efficient method for the preparation of optically active heterocyclic acids with excellent enantioselectivities. Copyright

3-AMINOETHYL-N-AMIDINO-2,5-DIHYDROPYRROLE DERIVATIVES HAVING ARGININE MIMETIC PROPERTIES

1The present invention ocncerns new amidinopyrroline derivatives of formula (I) with the meanings of the symbols as given in the description as well as a process for their production and their use in pharmaceutical preparations.