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1370641-48-7

(E)-3-(4-methoxyphenyl)-2-methylacryloyl chloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1370641-48-7 Structure

  • Basic information

    1. Product Name: (E)-3-(4-methoxyphenyl)-2-methylacryloyl chloride
    2. Synonyms: (E)-3-(4-methoxyphenyl)-2-methylacryloyl chloride
    3. CAS NO:1370641-48-7
    4. Molecular Formula:
    5. Molecular Weight: 210.66
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1370641-48-7.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: (E)-3-(4-methoxyphenyl)-2-methylacryloyl chloride(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-3-(4-methoxyphenyl)-2-methylacryloyl chloride(1370641-48-7)
    11. EPA Substance Registry System: (E)-3-(4-methoxyphenyl)-2-methylacryloyl chloride(1370641-48-7)

  • 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: 1370641-48-7(Hazardous Substances Data)

1370641-48-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1370641-48-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,0,6,4 and 1 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1370641-48:
(9*1)+(8*3)+(7*7)+(6*0)+(5*6)+(4*4)+(3*1)+(2*4)+(1*8)=147
147 % 10 = 7
So 1370641-48-7 is a valid CAS Registry Number.

1370641-48-7Relevant articles and documents

Macrolide Synthesis through Intramolecular Oxidative Cross-Coupling of Alkenes

Jiang, Bing,Zhao, Meng,Li, Shu-Sen,Xu, Yun-He,Loh, Teck-Peng

, p. 555 - 559 (2018)

A RhIII-catalyzed intramolecular oxidative cross-coupling between double bonds for the synthesis of macrolides is described. Under the optimized reaction conditions, macrocycles containing a diene moiety can be formed in reasonable yields and with excellent chemo- and stereoselectivity. This method provides an efficient approach to synthesize macrocyclic compounds containing a 1,3-conjugated diene structure.

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