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5717-41-9

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5717-41-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5717-41-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,1 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5717-41:
(6*5)+(5*7)+(4*1)+(3*7)+(2*4)+(1*1)=99
99 % 10 = 9
So 5717-41-9 is a valid CAS Registry Number.

5717-41-9 Well-known Company Product Price

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  • Aldrich

  • (736899)  Ethyl 2-methyl-2,3-butadienoate  

  • 5717-41-9

  • 736899-250MG

  • 1,187.55CNY

  • Detail

5717-41-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-methylbuta-2,3-dienoate

1.2 Other means of identification

Product number -
Other names 2-Methyl-2,3-butadiensaeure-ethylester

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:5717-41-9 SDS

5717-41-9Relevant articles and documents

A Short Synthesis of Allene- and Cumulenecarboxylates

Kohl-Mines, Elisabeth,Hansen, Hans-Juergen

, p. 2244 - 2248 (1985)

It is shown that carboxylic acids, in the presence of Bu3N and 2-chloro-1-methylpyridinium iodide in toluene or CH2Cl2, react with phosphoranes to yield the corresponding esters of allene carboxylic acids (cf.Scheme

Rhodium(III)-Catalyzed Annulative Coupling of Sulfoxonium Ylides and Allenoates: An Arene C-H Activation/Cyclopropanation Cascade

Lou, Jiang,Wang, Quannan,Zhou, Yong-Gui,Yu, Zhengkun

supporting information, p. 9217 - 9222 (2019/11/19)

Rhodium(III)-catalyzed annulative coupling of sulfoxonium ylides with allenoates was achieved, forming highly functionalized cyclopropanes with a quaternary carbon center by means of the sulfoxonium ylide functionality as a traceless bifunctional directin

Phosphine-Catalyzed [8 + 2]-Annulation of Heptafulvenes with Allenoates and Its Asymmetric Variant: Construction of Bicyclo[5.3.0]decane Scaffold

Gao, Zhenzhen,Wang, Chang,Zhou, Leijie,Yuan, Chunhao,Xiao, Yumei,Guo, Hongchao

supporting information, p. 4302 - 4305 (2018/07/29)

In this paper, a phosphine-catalyzed [8 + 2]-annulation of heptafulvene with allenoates has been achieved under mild conditions, giving functionalized bicyclo[5.3.0]decane derivatives in moderate to excellent yields. Using chiral phosphine as the catalyst, optically active products were obtained in moderate to high yields with excellent enantioselectivities.

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