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CAS

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134847-04-4

2-(2,4-Dichloro-phenoxy)-4-methyl-pent-4-enoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 134847-04-4 Structure

  • Basic information

    1. Product Name: 2-(2,4-Dichloro-phenoxy)-4-methyl-pent-4-enoic acid
    2. Synonyms:
    3. CAS NO:134847-04-4
    4. Molecular Formula:
    5. Molecular Weight: 275.131
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 134847-04-4.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: 2-(2,4-Dichloro-phenoxy)-4-methyl-pent-4-enoic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(2,4-Dichloro-phenoxy)-4-methyl-pent-4-enoic acid(134847-04-4)
    11. EPA Substance Registry System: 2-(2,4-Dichloro-phenoxy)-4-methyl-pent-4-enoic acid(134847-04-4)

  • 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: 134847-04-4(Hazardous Substances Data)

134847-04-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 134847-04-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,8,4 and 7 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 134847-04:
(8*1)+(7*3)+(6*4)+(5*8)+(4*4)+(3*7)+(2*0)+(1*4)=134
134 % 10 = 4
So 134847-04-4 is a valid CAS Registry Number.

134847-04-4Downstream Products

134847-04-4Relevant articles and documents

Synthesis of methyl 2-aryloxy-4-methyl-4-pentenoates and 2-aryloxy-4-methyl-4-pentenals

Fechtel,Westphal,Ruger,Matschiner

, p. 399 - 401 (2007/10/02)

A convenient procedure for the preparation of the title compounds from 1,1,1-trichloro-4-methyl-4-penten-2-ol (1) and 1,1-dichloro-4-methyl-4-penten-2-ol (8), respectively, by treatment with unsubstituted and substituted sodium phenolates 5 is described.

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