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Propanedioic acid, 3-butenyl-2-propenyl-, diethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51481-46-0

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51481-46-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51481-46-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,4,8 and 1 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 51481-46:
(7*5)+(6*1)+(5*4)+(4*8)+(3*1)+(2*4)+(1*6)=110
110 % 10 = 0
So 51481-46-0 is a valid CAS Registry Number.

51481-46-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-allyl-2-but-3-enyl-malonic acid diethyl ester

1.2 Other means of identification

Product number -
Other names diethyl 2-allyl-2-(but-3-en-1-yl)malonate

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:51481-46-0 SDS

51481-46-0Relevant academic research and scientific papers

A medium fluorous Grubbs-Hoveyda 2nd generation catalyst for phase transfer catalysis of ring closing metathesis reactions

Kobayashi, Yuki,Inukai, Sae,Kondo, Natsuki,Watanabe, Tomoko,Sugiyama, Yuya,Hamamoto, Hiromi,Shioiri, Takayuki,Matsugi, Masato

supporting information, p. 1363 - 1366 (2015/03/04)

A fluorous Grubbs-Hoveyda metathesis catalyst supported on Teflon powder, that readily moves between the solid phase (Teflon) and the liquid phase (DMF) was prepared. By modulating the hydrophobicity of the reaction medium at the end of the reaction, the supported catalyst could be recovered by simple filtration even though the catalyst existed in a homogeneous state during the reaction. In RCM reactions, the catalyst could be reused up to three times with only a slight loss in reactivity with each subsequent cycle.

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