4096-21-3 | 1-Phenylpyrrolidine

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	in stock	$10.00	$7.00
1g	95%	in stock	$23.00	$17.00
5g	95%	in stock	$43.00	$31.00
10g	95%	in stock	$85.00	$60.00
25g	95%	in stock	$211.00	$148.00
100g	95%	in stock	$650.00	$455.00

Description

• Catalog Number: AF56329
• Chemical Name: 1-Phenylpyrrolidine
• CAS Number: 4096-21-3
• Molecular Formula: C10H13N
• Molecular Weight: 147.2169
• MDL Number: MFCD00015897
• SMILES: C1CCN(C1)c1ccccc1
• NSC Number: 53425

Computed Properties

• Complexity: 110
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 3.6

Literature

• Structure and property based design of factor Xa inhibitors: pyrrolidin-2-ones with aminoindane and phenylpyrrolidine P4 motifs.

  Bioorganic & medicinal chemistry letters 20110315

• Optimization of phenyl-substituted benzimidazole carboxamide poly(ADP-ribose) polymerase inhibitors: identification of (S)-2-(2-fluoro-4-(pyrrolidin-2-yl)phenyl)-1H-benzimidazole-4-carboxamide (A-966492), a highly potent and efficacious inhibitor.

  Journal of medicinal chemistry 20100422

• (3S,4S)-1-Benzyl-pyrrolidine-3,4-diol.

  Acta crystallographica. Section E, Structure reports online 20100401

• Unexpectedly similar charge transfer rates through benzo-annulated bicyclo[2.2.2]octanes.

  Journal of the American Chemical Society 20080618

• Selective and catalytic arylation of N-phenylpyrrolidine: (sp3) C-H bond functionalization in the absence of a directing group [J. Am. Chem. Soc. 2005, 127, 5284-5285].

  Journal of the American Chemical Society 20060308

• Selective and catalytic arylation of N-phenylpyrrolidine: sp3 C-H bond functionalization in the absence of a directing group.

  Journal of the American Chemical Society 20050420

• Synthesis and biological evaluation of 3-(4-substituted-phenyl)-N-hydroxy-2-propenamides, a new class of histone deacetylase inhibitors.

  Journal of medicinal chemistry 20031218