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183011-14-5

2-propenoic acid, 3-(4-methoxyphenyl)-2-methyl-, butyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 183011-14-5 Structure

  • Basic information

    1. Product Name: 2-propenoic acid, 3-(4-methoxyphenyl)-2-methyl-, butyl ester
    2. Synonyms: Butyl 3-(4-methoxyphenyl)-2-methylacrylate
    3. CAS NO:183011-14-5
    4. Molecular Formula: C15H20O3
    5. Molecular Weight: 248.3175
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 183011-14-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 362.821°C at 760 mmHg
    3. Flash Point: 151.569°C
    4. Appearance: N/A
    5. Density: 1.034g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.525
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-propenoic acid, 3-(4-methoxyphenyl)-2-methyl-, butyl ester(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-propenoic acid, 3-(4-methoxyphenyl)-2-methyl-, butyl ester(183011-14-5)
    12. EPA Substance Registry System: 2-propenoic acid, 3-(4-methoxyphenyl)-2-methyl-, butyl ester(183011-14-5)

  • 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: 183011-14-5(Hazardous Substances Data)

183011-14-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 183011-14-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,0,1 and 1 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 183011-14:
(8*1)+(7*8)+(6*3)+(5*0)+(4*1)+(3*1)+(2*1)+(1*4)=95
95 % 10 = 5
So 183011-14-5 is a valid CAS Registry Number.

183011-14-5Downstream Products

183011-14-5Relevant articles and documents

A novel catalytic decarbonylative Heck-type reaction and conjugate addition of aldehydes to unsaturated carbonyl compounds

Yang, Luo,Correia, Camille A.,Guo, Xiangyu,Li, Chao-Jun

experimental part, p. 5486 - 5489 (2010/10/20)

A novel rhodium-catalyzed decarbonylative reaction of aldehydes with unsaturated carbonyl compounds was discovered to generate Heck-type reaction product and conjugate addition product.

Selective arylation of 1,1-disubstituted olefins using a biphenyl-based phosphine in Heck coupling reactions

Nadri, Shirin,Joshaghani, Mohammad,Rafiee, Ezzat

experimental part, p. 5470 - 5473 (2010/01/11)

The biphenyl-based phosphine, 2-diphenylphosphino-2′-methylbiphenyl is an effective ligand for palladium-catalyzed terminal arylation of 1,1-disubstituted olefins with aryl bromides in DMF and K2CO3 as base. The yields of products are independent of the electronic properties of the aryl bromides, however, the nature of the olefin has a major effect.

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