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mono-tert-butyl 2-(4-vinylbenzyl)malonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 324740-08-1 Structure
  • Basic information

    1. Product Name: mono-tert-butyl 2-(4-vinylbenzyl)malonate
    2. Synonyms: mono-tert-butyl 2-(4-vinylbenzyl)malonate
    3. CAS NO:324740-08-1
    4. Molecular Formula:
    5. Molecular Weight: 276.332
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 324740-08-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: mono-tert-butyl 2-(4-vinylbenzyl)malonate(CAS DataBase Reference)
    10. NIST Chemistry Reference: mono-tert-butyl 2-(4-vinylbenzyl)malonate(324740-08-1)
    11. EPA Substance Registry System: mono-tert-butyl 2-(4-vinylbenzyl)malonate(324740-08-1)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 324740-08-1(Hazardous Substances Data)

324740-08-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 324740-08-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,4,7,4 and 0 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 324740-08:
(8*3)+(7*2)+(6*4)+(5*7)+(4*4)+(3*0)+(2*0)+(1*8)=121
121 % 10 = 1
So 324740-08-1 is a valid CAS Registry Number.

324740-08-1Relevant articles and documents

Cobalt-Catalyzed Highly Regioselective Three-Component Arylcarboxylation of Acrylate with Aryl Bromides and Carbon Dioxide

Hang, Wei,Liang, Nianjie,Liu, Yuzhou,Xi, Chanjuan

, p. 4941 - 4946 (2021/10/30)

Cobalt-catalyzed regioselective three-component arylcarboxylation of acrylate with aryl bromides and carbon dioxide has been developed. The reaction is carried out by using cobalt chloride as a precatalyst and zinc powder as a reducing reagent under CO2 (1 atm) at 40 °C. A range of aryl bromides are used for this reaction, leading to a series of valuable carboxylic acids with high regioselectivity and functional-group compatibility. Mechanistic experiments and DFT calculations indicate that this arylcarboxylation reaction involves the reaction of CO2 with a cobalt enolate intermediate to form the C?C bond.

Toward environmentally friendly photolithographic materials: A new class of water-soluble photoresists

Yamada, Shintaro,Mrozek, Thomas,Rager, Timo,Owens, Jordan,Rangel, Jose,Willson, C. Grant,Byers, Jeffery

, p. 377 - 384 (2007/10/03)

New water-soluble styrenic polymers bearing two functional groups, pendant ammonium salts of half-esters of malonic acids and acid-labile alkyl esters, were synthesized and evaluated for water-soluble positive-tone photoresist application. These polymers feature two solubility switches: insolubilization of the entire film by baking and selective solubilization upon exposure to UV light. Time-resolved FT-IR measurement of the baked films showed sequential evaporation of ammonia from the films and the decarboxylation of the malonate half-esters. The rates of decarboxylation depend on the structure of substituents at the 2-position of the malonates. The choice of acid-labile esters, the structure of the half-esters, and the polymer compositions were carefully optimized, and high-resolution positive tone images were obtained that were fully processed in aqueous media.

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