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Ethyl 2-propylacrylate 99, also known as 2-propyl acrylate or 2-methylbutyl acrylate, is a colorless liquid with a molecular formula of C7H12O2. It is a monomeric ester derived from acrylic acid and 2-propanol, and is commonly used in the production of polymers, resins, and adhesives. This chemical is characterized by its strong, pungent odor and is considered flammable and hazardous. It is important to handle Ethyl 2-propylacrylate 99 with care, as it can cause irritation to the eyes, skin, and respiratory system, and may also be harmful if ingested or inhaled. Due to its reactivity, it is often used in the synthesis of various polymers and copolymers, contributing to its applications in coatings, textiles, and other industrial products.

3550-06-9

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3550-06-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3550-06-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,5 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3550-06:
(6*3)+(5*5)+(4*5)+(3*0)+(2*0)+(1*6)=69
69 % 10 = 9
So 3550-06-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H14O2/c1-4-6-7(3)8(9)10-5-2/h3-6H2,1-2H3

3550-06-9 Well-known Company Product Price

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  • Aldrich

  • (590118)  Ethyl2-propylacrylate  99%, contains 150 ppm BHT as inhibitor

  • 3550-06-9

  • 590118-250MG

  • 2,909.79CNY

  • Detail

3550-06-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-methylidenepentanoate

1.2 Other means of identification

Product number -
Other names Ethyl 2-propylacrylate

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:3550-06-9 SDS

3550-06-9Relevant academic research and scientific papers

One-pot asymmetric conjugate addition-trapping of zinc enolates by activated electrophiles

Rathgeb, Xavier,March, Sebastien,Alexakis, Alexandre

, p. 5737 - 5742 (2007/10/03)

The copper-catalyzed asymmetric conjugate addition of dialkyl zinc leads to homochiral zinc enolates. These intermediates were trapped in situ with activated allylic electrophiles, without the need of additional palladium catalysis. High trans selectivity

Preparation et etude de nouveaux derives organozinciques allyliques fonctionnels

Lambert, Francois,Kirschleger, Bernard,Villieras, Jean

, p. 273 - 286 (2007/10/02)

Stable organozinc compounds derived from alkyl-3-alkyl-2-(bromomethyl)-propenoates have been prepared.NMR 13C, 1H and IR studies show only one Z stereoisomer (no methylenic form) with a strong chelation between zinc and the carbonyl oxygen of the ester and solvated by only one solvent molecule.Hydrolysis can be achieved by two concurrent mechanisms with or without transposition.

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