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33240-23-2

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33240-23-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33240-23-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,2,4 and 0 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 33240-23:
(7*3)+(6*3)+(5*2)+(4*4)+(3*0)+(2*2)+(1*3)=72
72 % 10 = 2
So 33240-23-2 is a valid CAS Registry Number.

33240-23-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 3-(4-methoxyanilino)but-2-enoate

1.2 Other means of identification

Product number -
Other names 3-p-Anisidino-1-(4-methoxy-phenyl)-5-phenyl-1,5-dihydro-pyrrol-2-on

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:33240-23-2 SDS

33240-23-2Relevant articles and documents

Design, synthesis, and biological evaluation of AV6 derivatives as novel dual reactivators of latent HIV-1

Ao, Mingtao,Pan, Zhenrui,Qian, Yuqing,Tang, Bowen,Feng, Zeming,Fang, Hua,Wu, Zhen,Chen, Jingwei,Xue, Yuhua,Fang, Meijuan

, p. 17279 - 17292 (2018)

The "shock and kill" strategy might be a promising therapeutic approach for HIV/AIDS due to the existence of latent viral reservoirs. A major challenge of the "shock and kill" strategy arises from the general lack of clinically effective latency-reversing

Multicomponent reaction for the synthesis of highly functionalized piperidine scaffolds catalyzed by TMSI

Wu, Lisha,Yan, Shiqiang,Wang, Wensheng,Li, Yinta

, p. 4311 - 4322 (2020/07/13)

An efficient method for the synthesis of highly functionalized piperidines via one-pot domino reaction of β-ketoesters, aromatic aldehydes, and aromatic amines was reported. This multicomponent coupling was catalyzed by TMSI in methanol at room temperature, giving desired substituted pyridines in moderate to good yields.

Highly efficient and facile synthesis of β-enaminones catalyzed by diphenylammonium triflate

Zhao, Ting-Ting,Song, Jiang-Long,Hong, Feng-Qing,Xia, Jian-Sheng,Li, Jian-Jun

, p. 2857 - 2868 (2019/08/21)

Abstract: The catalytic performance of diphenylammonium triflates as an organocatalyst in the synthesis of β-enaminones from various substituted β-diketones and amides (or amines) were evaluated. A wide range of β-enaminones were efficiently synthesized in good to excellent yields under mild reaction conditions. Applying diphenylammonium triflate (DPAT) as catalyst makes this protocol cost-effective, low corrosive and easy to handle. Graphic abstract: [Figure not available: see fulltext.].

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