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(E)-3-chloro-1-(4-methoxyphenyl)oct-2-en-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1415426-07-1 Structure
  • Basic information

    1. Product Name: (E)-3-chloro-1-(4-methoxyphenyl)oct-2-en-1-one
    2. Synonyms: (E)-3-chloro-1-(4-methoxyphenyl)oct-2-en-1-one
    3. CAS NO:1415426-07-1
    4. Molecular Formula:
    5. Molecular Weight: 266.768
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1415426-07-1.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-chloro-1-(4-methoxyphenyl)oct-2-en-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-3-chloro-1-(4-methoxyphenyl)oct-2-en-1-one(1415426-07-1)
    11. EPA Substance Registry System: (E)-3-chloro-1-(4-methoxyphenyl)oct-2-en-1-one(1415426-07-1)
  • 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: 1415426-07-1(Hazardous Substances Data)

1415426-07-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1415426-07-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,5,4,2 and 6 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1415426-07:
(9*1)+(8*4)+(7*1)+(6*5)+(5*4)+(4*2)+(3*6)+(2*0)+(1*7)=131
131 % 10 = 1
So 1415426-07-1 is a valid CAS Registry Number.

1415426-07-1Relevant articles and documents

Divergent Halogenation Pathways of 2,2-Dichlorobut-3-yn-1-ols to 3-Chloro-4-Iodofurans and α-Chloro-γ-Iodoallenes: Electrophilic versus Pd(II)-Catalyzed Halogenation Strategies

Abozeid, Mohamed Ahmed,Kim, Hun Young,Oh, Kyungsoo

, p. 5368 - 5373 (2020)

Divergent halogenation pathways of 2,2-dichlorobut-3-yn-1-ols have been developed to give 3,4-dihalofurans and 1,3-dihaloallenyl ketones in good to excellent yields. Thus, the readily accessible 2,2-dichlorobut-3-yn-1-ols were treated with the electrophil

Studies on elimination pathways of β-halovinyl ketones leading to allenyl and propargyl ketones and furans under the action of mild bases

Kim, Hun Young,Li, Jian-Yuan,Oh, Kyungsoo

, p. 11132 - 11145 (2013/02/23)

The elimination pathway of stereochemically defined β-halovinyl ketones has been investigated using a mild base, NEt3, leading to the formation of allenyl ketones and propargyl ketones. A preferential α-vinyl enolization of (E)-β-chlorovinyl ke

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