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999-21-3

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999-21-3 Usage

Chemical Properties

colorless liquid with a pungent odor.

Uses

Different sources of media describe the Uses of 999-21-3 differently. You can refer to the following data:
1. An agent for the promotion of branching in emulsion polymers
2. Diallyl maleate has potential applications in polyester resins, adhesives, and ion exchange resins. When used at low levels, Diallyl Maleate is an effective agent for the promotion of branching in emulsion polymers.

Preparation

Diallyl maleate is obtained by the sulfuric acid-catalyzed esterification of maleic anhydride with propyl alcohol.

Safety Profile

Poison by ingestion and intraperitoneal routes. Moderately toxic by skin contact. A skin and eye irritant. When heated to decomposition it emits acrid smoke and irritating fumes. See also ALLYL COMPOUNDS and ESTERS.

Check Digit Verification of cas no

The CAS Registry Mumber 999-21-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,9 and 9 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 999-21:
(5*9)+(4*9)+(3*9)+(2*2)+(1*1)=113
113 % 10 = 3
So 999-21-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O4/c1-3-7-13-9(11)5-6-10(12)14-8-4-2/h3-6H,1-2,7-8H2/b6-5-

999-21-3 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (L03867)  Diallyl maleate, 95%   

  • 999-21-3

  • 50g

  • 230.0CNY

  • Detail
  • Alfa Aesar

  • (L03867)  Diallyl maleate, 95%   

  • 999-21-3

  • 250g

  • 707.0CNY

  • Detail
  • Alfa Aesar

  • (L03867)  Diallyl maleate, 95%   

  • 999-21-3

  • 1000g

  • 1966.0CNY

  • Detail
  • Aldrich

  • (291226)  Diallylmaleate  technical grade, 93%

  • 999-21-3

  • 291226-250ML

  • 1,886.04CNY

  • Detail

999-21-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Diallyl maleate

1.2 Other means of identification

Product number -
Other names DIALLYL MALEATE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Intermediates
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:999-21-3 SDS

999-21-3Relevant articles and documents

Synthesis and characterization of a new hydroxyl functionalized diacidic ionic liquid as catalyst for the preparation of diester plasticizers

Fareghi-Alamdari, Reza,Nadiri Niri, Mehri,Hazarkhani, Hassan

, p. 153 - 160 (2016/12/30)

Two new functionalized diacidic ionic liquids (FDAILs) including hydroxyl functionalized diacidic ionic liquid (HFDAIL) and sulfonated diacidic ionic liquid (SFDAIL) were synthesized and characterized by 1HNMR, 13CNMR and FT-IR. The catalytic activities of these FDAILs were examined in esterification reaction of anhydrides with some alcohols to give corresponding dialkyl plasticizers under solvent-free conditions. The results indicate that HFDAIL, as hydroxyl-bearing catalyst, show better catalytic performance. Under the optimum conditions, using HFDAIL, the conversion of phthalic anhydride was high and diester plasticizers were obtained with good to excellent yields in the presence of only 10?mol% of ionic liquid. All the produced diesters could be easily recovered due to their immiscibility with the ionic liquid. Recycling experiments suggests that these ionic liquids can be reused several times without remarkable loss in their catalytic activity.

Titanium isopropoxide promoted tandem self-cross and ring-closing metathesis approach for the synthesis of macrotetralides

Muthusamy, Sengodagounder,Azhagan, Datshanamoorthy

, p. 363 - 370 (2014/01/23)

A new approach is demonstrated for the synthesis of macrotetralides through an olefin metathesis reaction using Grubbs' second-generation catalyst with titanium isopropoxide as a cocatalyst. This study demonstrates a tandem self-cross and ring-closing metathesis approach to form macrocyclic ring systems with excellent (E) selectivity. The reaction was optimized with regard to functional group, catalyst, solvent, Lewis acid, concentration, and temperature. A new approach is demonstrated for the synthesis of macrotetralides through tandem self-cross and ring-closing metathesis reactions using Grubbs' second-generation catalyst and titanium isopropoxide. Copyright

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