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CAS

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136138-66-4

methyl α-methoxy-β-(β-pyridyl)acrylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 136138-66-4 Structure

  • Basic information

    1. Product Name: methyl α-methoxy-β-(β-pyridyl)acrylate
    2. Synonyms: methyl α-methoxy-β-(β-pyridyl)acrylate
    3. CAS NO:136138-66-4
    4. Molecular Formula:
    5. Molecular Weight: 193.202
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 136138-66-4.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: methyl α-methoxy-β-(β-pyridyl)acrylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl α-methoxy-β-(β-pyridyl)acrylate(136138-66-4)
    11. EPA Substance Registry System: methyl α-methoxy-β-(β-pyridyl)acrylate(136138-66-4)

  • 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: 136138-66-4(Hazardous Substances Data)

136138-66-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 136138-66-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,1,3 and 8 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 136138-66:
(8*1)+(7*3)+(6*6)+(5*1)+(4*3)+(3*8)+(2*6)+(1*6)=124
124 % 10 = 4
So 136138-66-4 is a valid CAS Registry Number.

136138-66-4Downstream Products

136138-66-4Relevant articles and documents

Studies on the synthesis of Strychnos indole alkaloids

Bosch,Salas,Amat,Alvarez,Morgo,Adrover

, p. 5269 - 5276 (2007/10/02)

Tetracycles 3b-d, having the ABCD ring substructure of Strychnos alkaloids and a N(b)-(formylmethyl) substituent protected as an oxime or hydrazone derivative, have been prepared by nucleophilic addition of the enolate of indoleacetic ester 1 to pyridinium salts 2b-d followed by acid cyclization. The same one-pot, two-step sequence allowed the preparation of tetracycle 3f, which incorporates an α-methoxyacrylate chain at the piperidine β-position.

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