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3509-01-1

4-Pentenoic acid, 2-cyano-, ethyl ester is a chemical compound with the molecular formula C8H11NO2. It is an ester derivative of 2-cyano-4-pentenoic acid, where the carboxylic acid group is esterified with ethanol. This organic compound is characterized by the presence of a cyano group (-CN) at the 2-position and a double bond in the 4-pentenoic acid backbone. It is a colorless liquid with a pungent odor and is soluble in organic solvents. 4-Pentenoic acid, 2-cyano-, ethyl ester has potential applications in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals due to its unique functional groups and reactivity. However, it should be handled with care, as it may have toxic or hazardous properties, and appropriate safety measures should be taken during its use and storage.

3509-01-1

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3509-01-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3509-01-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,0 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3509-01:
(6*3)+(5*5)+(4*0)+(3*9)+(2*0)+(1*1)=71
71 % 10 = 1
So 3509-01-1 is a valid CAS Registry Number.

3509-01-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl α-allyl-α-cyanoacetate

1.2 Other means of identification

Product number -
Other names ethyl α-allylcyanoacetate

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:3509-01-1 SDS

3509-01-1Downstream Products

3509-01-1Relevant articles and documents

Reactions d'alkylation de Fe(CO)2(NO) (η3-propenyl) par des nucleophiles carbones. Nature de l'intermediaire reactionnel

Roustan, Jean-Louis A.,Houlihan, Francois

, p. 215 - 220 (2007/10/02)

Decomposition of the intermediate resulting from the reaction of Fe(CO)2(NO)(η3-propenyl) (1) with a nucleophile -CH(CO2Et) (A) (2i A=CO2Et, i=1; A=CN, i=2) has been carried out under a variety of conditions using in particular two nucleophiles added, respectively, before and after the formation of the intermediate.The composition of the mixture of alkylation products obtained suggests that reaction of 1 with 2i is reversibly by complexation of the nucleophile with a concomitant η3 to η1 conversion of the allyl ligand.

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