Product Added to Cart!
(S)-2-[[3,5-Bis(trifluoromethyl)phenyl]thioureido]-N-benzyl-N,3,3-trimethylbutanamide, 95%, (98% ee)|07-1417|959979-30-7

(S)-2-[[3,5-Bis(trifluoromethyl)phenyl]thioureido]-N-benzyl-N,3,3-trimethylbutanamide, 95%, (98% ee)

$101.00

FREE
SHIPPING

100% MONEY
BACK GUARANTEE

ONLINE
SUPPORT 24/7

Available on backorder. No lead time available. Please request a quote.
Sku SC07-1417_100_MG
US-Strem
Get Bulk Quote

Product Information

Product Name
(S)-2-3,5-Bis(trifluoromethyl)phenylthioureido-N-benzyl-N,3,3-trimethylbutanamide, 95%, (98% ee)
Brand Name
US-Strem
Product Number
07-1417
CAS
959979-30-7
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
44541120
IUPAC Name
(2S)-N-benzyl-2-3,5-bis(trifluoromethyl)phenylcarbamothioylamino-N,3,3-trimethylbutanamide
InChI Key
LTFFYVVCUVYZPE-GOSISDBHSA-N
SMILES
CC(C)(C)C@@H(C(=O)N(C)CC1=CC=CC=C1)NC(=S)NC2=CC(=CC(=C2)C(F)(F)F)C(F)(F)F

Description

Technical Notes:
1.aza-MichaeI Reaction - Catalyst for the formal addition of ammonia to nitroalkenes, affording optically active
ß-amino nitro compounds in high yields and enantioselectivities. The approach is based on a novel thiourea- catalyzed aza-MichaeI reaction, by which benzophenone imine serves as a masked ammonia equiv., which is released by hydrolysis.
2.Diels-Alder Reaction - A variety of organocatalysts were screened for the catalysis of the naphthoquinone monoketal Diels-Alder reaction.
References:
1.Chem.-Eur. J., 2010, 16, 13330-13334
2. Beilstein J. Org. Chem., 2013, 9, 1414-1418.

References Data Source From Pubchem

Activation Modes in Asymmetric Anion-Binding Catalysis
Publication Name: Synthesis
Publication Date: 2022-07-27
DOI: 10.1055/a-1846-6139

l-Proline Derived Secondary Aminothiourea Organocatalyst for Synthesis of Coumarin Derived Trisubstituted Methanes: Rate Enhancement by Bifunctional Catalyst over Cooperative Catalysis
Publication Name: Catalysis Letters
Publication Date: 2019-05-16
DOI: 10.1007/s10562-019-02809-4

Nucleophilic Catalysis with Ion-Pair Catalysis
Publication Name: Science of Synthesis
Publication Date: 2019

A Continuous-Flow, Two-Step, Metal-Free Process for the Synthesis of Differently Substituted Chiral 1,2-Diamino Derivatives
Publication Name: Synthesis
Publication Date: 2018-02-01
DOI: 10.1055/s-0036-1591911

Lewis Base Catalysis of Three n–π* Mediated Reactions with N-Heterocyclic Carbenes (NHCs), Isothioureas, Bicyclic Tertiary Amines, and Electron-Rich Pyridyls
Publication Name: Synthesis
Publication Date: 2014-06-12
DOI: 10.1055/s-0033-1338653