116558-84-0

Basic information

• Product Name: (+/-)-trans-2-butyl-5-heptylpyrrolidine
• Synonyms: (+/-)-trans-2-butyl-5-heptylpyrrolidine
• CAS NO: 116558-84-0
• Molecular Weight: 225.418
• Mol File: 116558-84-0.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: (+/-)-trans-2-butyl-5-heptylpyrrolidine(CAS DataBase Reference)
• NIST Chemistry Reference: (+/-)-trans-2-butyl-5-heptylpyrrolidine(116558-84-0)
• EPA Substance Registry System: (+/-)-trans-2-butyl-5-heptylpyrrolidine(116558-84-0)

Safety Data

• Hazardous Substances Data: 116558-84-0(Hazardous Substances Data)

Upstream product

• 128741-69-5 C₁₇H₃₁NO₄ 
• 129398-05-6 (2R,5R)-2-Butyl-5-heptyl-pyrrolidine-1-carboxylic acid methyl ester 
• 123993-98-6 trans-N-(p-tolylsulfonyl)-2-heptyl-5-butylpyrrolidine 
• 116558-82-8 5-butyl-2-heptyl-3,4-dihydro-2H-pyrrol 
• 18356-28-0 tetrahydro-pyrrolizin-3,5-dione 
• 2405-92-7 pyrrolidin-2-one, 5-heptyl- 
• 116454-75-2 5-heptylpyrrolidine-2-thione 
• 116454-69-4 5-(3'-oxoheptyl)pyrrolidin-2-one 
• 116454-71-8 5-<3',3'-(ethylenedithio)heptyl>pyrrolidin-2-one 
• 116454-77-4 2-heptyl-3,4-dihydro-5-thyiomethyl-2H-Pyrrol 
• 1258206-78-8 8-azidopentadecan-5-one 
• 129397-98-4 (5R)-5-Heptyl-1-methoxycarbonyl-L-proline methyl ester 
• 129398-01-2 (R)-2-Heptyl-5-methoxy-pyrrolidine-1-carboxylic acid methyl ester 
• 50965-97-4 heptylcopper 

Downstream Products

• 95513-29-4 (2R,5R)-1-Benzenesulfonyl-2-butyl-5-heptyl-pyrrolidine 

Relevant articles and documents

(2R-trans)-2-Butyl-5-heptylpyrrolidine as a potent sigma receptor ligand produced by Streptomyces longispororuber

A potent sigma (σ) receptor ligand was isolated from the culture broth of Streptomyces longispororuber 525. The active compound was identified to be (2R-trans)-2-butyl-5-heptylpyrrolidine by spectroscopic and chemical studies. The compound exhibited high affinity and selectivity for σ receptors. The IC50 values toward σ1, σ2 and dopamine D2 receptors were 2.0, 22.7 and more than 40,000 nM, respectively. Its (2S-trans)- and (±)-cis-isomers, both synthesized, were also found to be high affinity σ ligands.

Efficient carboazidation of alkenes using a radical desulfonylative azide transfer process

The radical-mediated carboazidation of terminal alkenes using electrophilic alkanesulfonyl azides is reported. A single reagent delivers the necessary electrophilic alkyl radical as well as the azido group, and good yields are obtained by using a moderate excess of the carboazidating reagent (1.5-2 equiv). Interestingly, in addition to the starting sulfonyl azide, this method requires only the use of a radical initiator, di-tert-butyldiazene. In terms of atom economy, this azide transfer reaction is close to ideal, as SO2 (1 equiv) is the only side product. The synthetic potential of this process has been demonstrated by a formal synthesis of the alkaloid lepadiformine C.

A Stereocontrolled Organopalladium Route to 2,5-Disubstituted Pyrrolidine Derivatives. Application to the Synthesis of a Venom Alkaloid of the Ant Species Monomorium latinode

A general method for the preparation of cis- and trans-2,5-disubstituted pyrrolidines from conjugated dienes has been developed.The approach involves a stereocontrolled syn- or anti-1,4-addition of an amino and an oxygen function to the diene via palladiu