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1228955-03-0

2-(3-methoxybenzyl)-3-phenylacrylic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1228955-03-0 Structure

  • Basic information

    1. Product Name: 2-(3-methoxybenzyl)-3-phenylacrylic acid methyl ester
    2. Synonyms: 2-(3-methoxybenzyl)-3-phenylacrylic acid methyl ester
    3. CAS NO:1228955-03-0
    4. Molecular Formula:
    5. Molecular Weight: 282.339
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1228955-03-0.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: 2-(3-methoxybenzyl)-3-phenylacrylic acid methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(3-methoxybenzyl)-3-phenylacrylic acid methyl ester(1228955-03-0)
    11. EPA Substance Registry System: 2-(3-methoxybenzyl)-3-phenylacrylic acid methyl ester(1228955-03-0)

  • 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: 1228955-03-0(Hazardous Substances Data)

1228955-03-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1228955-03-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,8,9,5 and 5 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1228955-03:
(9*1)+(8*2)+(7*2)+(6*8)+(5*9)+(4*5)+(3*5)+(2*0)+(1*3)=170
170 % 10 = 0
So 1228955-03-0 is a valid CAS Registry Number.

1228955-03-0Downstream Products

1228955-03-0Relevant articles and documents

Pd(0)-catalyzed couplings using bromide and chloride derivatives of Baylis-Hillman adducts with triarylbismuths as atom-efficient multi-coupling nucleophiles

Rao, Maddali L.N.,Banerjee, Debasis,Dhanorkar, Ritesh J.

experimental part, p. 3623 - 3632 (2010/07/02)

Bromide and chloride derivatives of Baylis-Hillman adducts have been demonstrated to react efficiently with triarylbismuths affording allylic arylated products in high yields under palladium-catalyzed conditions. Triarylbismuths have been employed in sub-stoichiometric amounts as multi-coupling and atom-efficient nucleophiles in these reactions. The reactivity of both allylic bromides and chlorides was found to be facile and equally efficient in couplings with triarylbismuths.

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