(S)-(-)-2-(Diphenylmethyl)pyrrolidine, 97%

Name: (S)-(-)-2-(Diphenylmethyl)pyrrolidine, 97% | 119237-64-8
Brand: J&K Chemical
SKU: JK167670_1_G
Price: 240.1 USD
Availability: OutOfStock

Cat. No JK167670_1_G

Vendor: J&K Chemical

Product Information

Product Name

(S)-(-)-2-(Diphenylmethyl)pyrrolidine, 97%

Brand Name

J&K

Product Number

167670

CAS

119237-64-8

SDS Document

View/Download

Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

2734053

IUPAC Name

(2S)-2-benzhydrylpyrrolidine

InChI Key

OXOBKZZXZVFOBB-INIZCTEOSA-N

SMILES

C1CC@H(NC1)C(C2=CC=CC=C2)C3=CC=CC=C3

Safety Information

Storage Condition

Store at 2-8℃

References Data Source From Pubchem

Inhibition of 14-3-3/Tau by Hybrid Small-Molecule Peptides Operating via Two Different Binding Modes

Publication Name: ACS Chemical Neuroscience

Publication Date: 2018-05-03

DOI: 10.1021/acschemneuro.8b00118

Dual Iminium- and Lewis Base Catalyzed Morita–Baylis–Hillman Reaction on Cyclopent-2-enone

Publication Name: Synlett

Publication Date: 2017-12-13

DOI: 10.1055/s-0036-1591521

The Diamino Analogues of Privileged Corey–Bakshi–Shibata and Jørgensen–Hayashi Catalysts: A Comparison of Their Performance

Publication Name: Synthesis

Publication Date: 2016-09-01

DOI: 10.1055/s-0035-1562793

A Fluorinated ”Designer'Organocatalyst

Publication Name: Synfacts

Publication Date: 2009-05-25

DOI: 10.1055/s-0029-1216770

Organocatalytic Formation of Quaternary Stereocenters

Publication Name: Synthesis

Publication Date: 2009-05

DOI: 10.1055/s-0029-1216796

(S)-(-)-2-(Diphenylmethyl)pyrrolidine, 97%

Product Information

General Information

Safety Information

References Data Source From Pubchem

Inhibition of 14-3-3/Tau by Hybrid Small-Molecule Peptides Operating via Two Different Binding Modes

Dual Iminium- and Lewis Base Catalyzed Morita–Baylis–Hillman Reaction on Cyclopent-2-enone

The Diamino Analogues of Privileged Corey–Bakshi–Shibata and Jørgensen–Hayashi Catalysts: A Comparison of Their Performance

A Fluorinated ”Designer'Organocatalyst

Organocatalytic Formation of Quaternary Stereocenters