29897-82-3 | 1-Benzyl-pyrrolidine

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	in stock	$8.00	$6.00
5g	98%	in stock	$65.00	$45.00
10g	95%	in stock	$70.00	$49.00

Description

• Catalog Number: AF28183
• Chemical Name: 1-Benzyl-pyrrolidine
• CAS Number: 29897-82-3
• Molecular Formula: C11H15N
• Molecular Weight: 161.2435
• MDL Number: MFCD00127807
• SMILES: C1CCN(C1)Cc1ccccc1

Computed Properties

• Complexity: 121
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 2
• XLogP3: 2.2

Literature

• 7-Azabicyclo[2.2.1]heptane as a scaffold for the development of selective sigma-2 (σ2) receptor ligands.

  Bioorganic & medicinal chemistry letters 20120615

• Evolving P450pyr hydroxylase for highly enantioselective hydroxylation at non-activated carbon atom.

  Chemical communications (Cambridge, England) 20120514

• Synthesis of Zn-containing microporous aluminophosphate with the STA-1 structure.

  Dalton transactions (Cambridge, England : 2003) 20110828

• Molecular insights into the self-aggregation of aromatic molecules in the synthesis of nanoporous aluminophosphates: a multilevel approach.

  Journal of the American Chemical Society 20091118

• Antitumor compounds from marine actinomycetes.

  Marine drugs 20090601

• Insights into structure direction of microporous aluminophosphates: competition between organic molecules and water.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20090101

• Supramolecular chemistry in the structure direction of microporous materials from aromatic structure-directing agents.

  Journal of the American Chemical Society 20081008

• Streptopyrrolidine, an angiogenesis inhibitor from a marine-derived Streptomyces sp. KORDI-3973.

  Phytochemistry 20080901

• 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

• Computational study of the structure-directing effect of benzylpyrrolidine and its fluorinated derivatives in the synthesis of the aluminophosphate ALPO-5.

  Journal of the American Chemical Society 20040929

• Preparation of (R)- and (S)-N-protected 3-hydroxypyrrolidines by hydroxylation with Sphingomonas sp. HXN-200, a highly active, regio- and stereoselective, and easy to handle biocatalyst.

  The Journal of organic chemistry 20011214