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145742-36-5

3,4-dichloro-2-methoxybenzaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 145742-36-5 Structure

  • Basic information

    1. Product Name: 3,4-dichloro-2-methoxybenzaldehyde
    2. Synonyms: 3,4-dichloro-2-methoxybenzaldehyde
    3. CAS NO:145742-36-5
    4. Molecular Formula:
    5. Molecular Weight: 205.04
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 145742-36-5.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: 3,4-dichloro-2-methoxybenzaldehyde(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,4-dichloro-2-methoxybenzaldehyde(145742-36-5)
    11. EPA Substance Registry System: 3,4-dichloro-2-methoxybenzaldehyde(145742-36-5)

  • 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: 145742-36-5(Hazardous Substances Data)

145742-36-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 145742-36-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,7,4 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 145742-36:
(8*1)+(7*4)+(6*5)+(5*7)+(4*4)+(3*2)+(2*3)+(1*6)=135
135 % 10 = 5
So 145742-36-5 is a valid CAS Registry Number.

145742-36-5Relevant articles and documents

Design, synthesis, and monoamine transporter binding site affinities of methoxy derivatives of indatraline

Gu,Yu,Jacobson,Rothman,Dersch,George,Flippen-Anderson,Rice

, p. 4868 - 4876 (2007/10/03)

A series of methoxy-containing derivatives of indatraline 13a-f and 17 were synthesized, and their binding affinities for the dopamine, serotonin, and norepinephrine transporter binding sites were determined. Introduction of a methoxy group to indatraline

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