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2-Butenoic acid, 4-[3,3-dimethyl-5-oxo-2-(phenylmethyl)-1-pyrazolidinyl]-4-oxo-, ethyl ester, (2E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

657395-59-0

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657395-59-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 657395-59-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,7,3,9 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 657395-59:
(8*6)+(7*5)+(6*7)+(5*3)+(4*9)+(3*5)+(2*5)+(1*9)=210
210 % 10 = 0
So 657395-59-0 is a valid CAS Registry Number.

657395-59-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-2-[(E)-3-(ethoxycarbonyl)propenoyl]-5,5-dimethyl-pyrazolidin-3-one

1.2 Other means of identification

Product number -
Other names (E)-4-(2-Benzyl-3,3-dimethyl-5-oxo-pyrazolidin-1-yl)-4-oxo-but-2-enoic acid ethyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:657395-59-0 SDS

657395-59-0Relevant academic research and scientific papers

Enantioselective Synthesis of N-Alkylamines through β-Amino C-H Functionalization Promoted by Cooperative Actions of B(C6F5)3and a Chiral Lewis Acid Co-Catalyst

Chang, Yejin,Cao, Min,Chan, Jessica Z.,Zhao, Cunyuan,Wang, Yuankai,Yang, Rose,Wasa, Masayuki

supporting information, p. 2441 - 2455 (2021/02/16)

We disclose a catalytic method for β-C(sp3)-H functionalization of N-alkylamines for the synthesis of enantiomerically enriched β-substituted amines, entities prevalent in pharmaceutical compounds and used to generate different families of chiral catalysts. We demonstrate that a catalyst system comprising of seemingly competitive Lewis acids, B(C6F5)3, and a chiral Mg- or Sc-based complex, promotes the highly enantioselective union of N-alkylamines and α,β-unsaturated compounds. An array of δ-amino carbonyl compounds was synthesized under redox-neutral conditions by enantioselective reaction of a N-alkylamine-derived enamine and an electrophile activated by the chiral Lewis acid co-catalyst. The utility of the approach is highlighted by late-stage β-C-H functionalization of bioactive amines. Investigations in regard to the mechanistic nuances of the catalytic processes are described.

Chiral Lewis Acid Catalysis in Nitrile Oxide Cycloadditions

Sibi, Mukund P.,Itoh, Kennosuke,Jasperse, Craig P.

, p. 5366 - 5367 (2007/10/03)

We describe examples of highly regio- and enantioselective nitrile oxide cycloadditions to unsaturated alkenes using substoichiometric amounts of a chiral Lewis acid. Pyrazolidinones proved to be effective achiral templates in the cycloadditions providing

Exo Selective Enantioselective Nitrone Cycloadditions

Sibi, Mukund P.,Ma, Zhihua,Jasperse, Craig P.

, p. 718 - 719 (2007/10/03)

We have developed a novel method for accessing exo adducts with high enantioselectivity in nitrone cycloadditions to enoates. Pyrazolidinones proved to be effective achiral templates in the cycloadditions, providing exo adducts typically in >15:1 selectivity and 90-98% ee. The use of Lewis acids that form square planar complexes, such as copper triflate, was important for obtaining high exo selectivity. Copyright

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