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14301-30-5

dichloro-acetic acid-(3,4-dimethoxy-phenethylamide) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 14301-30-5 Structure

  • Basic information

    1. Product Name: dichloro-acetic acid-(3,4-dimethoxy-phenethylamide)
    2. Synonyms: dichloro-acetic acid-(3,4-dimethoxy-phenethylamide)
    3. CAS NO:14301-30-5
    4. Molecular Formula:
    5. Molecular Weight: 292.162
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 14301-30-5.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: dichloro-acetic acid-(3,4-dimethoxy-phenethylamide)(CAS DataBase Reference)
    10. NIST Chemistry Reference: dichloro-acetic acid-(3,4-dimethoxy-phenethylamide)(14301-30-5)
    11. EPA Substance Registry System: dichloro-acetic acid-(3,4-dimethoxy-phenethylamide)(14301-30-5)

  • 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: 14301-30-5(Hazardous Substances Data)

14301-30-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14301-30-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,3,0 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 14301-30:
(7*1)+(6*4)+(5*3)+(4*0)+(3*1)+(2*3)+(1*0)=55
55 % 10 = 5
So 14301-30-5 is a valid CAS Registry Number.

14301-30-5Relevant articles and documents

THE INTERMOLECULAR BENZYNE CYCLOADDITION (IBC) APPROACH TO 7-SUBSTITUTED APORPHINOIDS.MECHANISTIC CONSIDERATIONS

Atanes, N.,Castedo, L.,Cobas, A.,Guitian, E.,Saa, C.,Saa, J. M.

, p. 7947 - 7956 (1989)

7-Alkyl-substituted aporphinoids were obtained in moderate yield through the reaction of N-protected 1-ethylidene-1,2,3,4-tetrahydroisoquinolines with benzyne. 7-Alkoxy and 7-chloro derivatives were also prepared by this route, though in lower yield.Mecha

Synthesis of some azeto[2,1-a]isoquinolin-2-ones

Cho, Su-Dong,Kim, Sung-Kyu,Yoon, Yong-Jin

, p. 77 - 80 (1998)

Some azeto[2,1-a]isoquinolin-2-ones were synthesized from 2-(3,4- dimethoxyphenyl)ethylamine in three steps in good yield.

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