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2-(ethylthio)ethyl acrylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15205-68-2

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15205-68-2 Usage

Physical Appearance

Clear, colorless liquid

Odor

Pungent

Flammability

Highly flammable

Polymerization Rate

Fast

Uses

Production of adhesives, coatings, and polymers; manufacturing of pressure-sensitive adhesives and emulsion polymers; as a monomer in the production of copolymers and resins; cross-linking with other compounds to form durable and flexible materials

Hazards

Can be hazardous if not handled properly

Safety

Should be stored and handled according to safety guidelines to prevent accidents and exposure.

Check Digit Verification of cas no

The CAS Registry Mumber 15205-68-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,2,0 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 15205-68:
(7*1)+(6*5)+(5*2)+(4*0)+(3*5)+(2*6)+(1*8)=82
82 % 10 = 2
So 15205-68-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H12O2S/c1-3-7(8)9-5-6-10-4-2/h3H,1,4-6H2,2H3

15205-68-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethylsulfanylethyl prop-2-enoate

1.2 Other means of identification

Product number -
Other names Acrylic acid ethylthioethyl ester

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:15205-68-2 SDS

15205-68-2Upstream product

15205-68-2Downstream Products

15205-68-2Relevant academic research and scientific papers

A new method using 2-chloro-4,6-dimethoxy-1,3,5-triazine for facile elimination of dimethylamino group in Eschenmoser's methylenation for synthesis of α,β-unsaturated esters

Yamada, Kohei,Masaki, Kazumasa,Hagimoto, Yuri,Kamiya, Seina,Kunishima, Munetaka

supporting information, p. 1758 - 1760 (2013/03/29)

A facile one-step method for the elimination of the dimethylamino group in Eschenmoser's methylenation has been developed using a combination of 2-chloro-4,6-dimethoxy-1,3,5-triazine and triethylamine. The chemoselective elimination of the dimethylamino group occurred in compounds possessing either a diethylamino group or an alkylsulfanyl group.

(METH)ACRYLIC ACID ESTER, ACTIVATION ENERGY RAY CURING COMPOSITION, AND INKJET RECORDING INK

-

Paragraph 0105; 0106; 0107; 0153; 0154, (2013/06/26)

(Meth)acrylic acid ester, which contains one or more partial structures each represented by the following formula 1 in a molecule thereof, wherein the partial structure is a urethane structure which does not have a hydrogen atom directly bonded to a nitrogen atom of the following formula 1: where the nitrogen atom is not bonded to a hydrogen atom.

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