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CAS

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1404433-17-5

ethyl (E)-α-bromo-3,5-dimethoxycinnamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1404433-17-5 Structure

  • Basic information

    1. Product Name: ethyl (E)-α-bromo-3,5-dimethoxycinnamate
    2. Synonyms:
    3. CAS NO:1404433-17-5
    4. Molecular Formula:
    5. Molecular Weight: 315.164
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1404433-17-5.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: ethyl (E)-α-bromo-3,5-dimethoxycinnamate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl (E)-α-bromo-3,5-dimethoxycinnamate(1404433-17-5)
    11. EPA Substance Registry System: ethyl (E)-α-bromo-3,5-dimethoxycinnamate(1404433-17-5)

  • 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: 1404433-17-5(Hazardous Substances Data)

1404433-17-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1404433-17-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,4,4,3 and 3 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1404433-17:
(9*1)+(8*4)+(7*0)+(6*4)+(5*4)+(4*3)+(3*3)+(2*1)+(1*7)=115
115 % 10 = 5
So 1404433-17-5 is a valid CAS Registry Number.

1404433-17-5Downstream Products

1404433-17-5Relevant articles and documents

Synthesis of naphthalenes via platinum-catalyzed hydroarylation of aryl enynes?

Kang, Dongjin,Kim, Jinsik,Oh, Susung,Lee, Phil Ho

, p. 5636 - 5639 (2012)

An efficient synthetic method of functionalized naphthalenes having hydrogen, alkyl, alkenyl, aryl, or heteroaryl groups on the 4-position and ethoxycarbonyl group on the 2-position was developed through selective Pt-catalyzed 6-endo intramolecular hydroa

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