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Acetic acid, trichloro-, 1-[(phenylmethoxy)methyl]-2-propenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 93553-67-4 Structure
  • Basic information

    1. Product Name: Acetic acid, trichloro-, 1-[(phenylmethoxy)methyl]-2-propenyl ester
    2. Synonyms:
    3. CAS NO:93553-67-4
    4. Molecular Formula: C13H13Cl3O3
    5. Molecular Weight: 323.603
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 93553-67-4.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: Acetic acid, trichloro-, 1-[(phenylmethoxy)methyl]-2-propenyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Acetic acid, trichloro-, 1-[(phenylmethoxy)methyl]-2-propenyl ester(93553-67-4)
    11. EPA Substance Registry System: Acetic acid, trichloro-, 1-[(phenylmethoxy)methyl]-2-propenyl ester(93553-67-4)
  • 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: 93553-67-4(Hazardous Substances Data)

93553-67-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93553-67-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,5,5 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 93553-67:
(7*9)+(6*3)+(5*5)+(4*5)+(3*3)+(2*6)+(1*7)=154
154 % 10 = 4
So 93553-67-4 is a valid CAS Registry Number.

93553-67-4Relevant articles and documents

FORMATION AND REACTIONS OF TRICHLORO-γ-LACTONES

Takano, Seiichi,Nishizawa, Shin'ichi,Akiyama, Masashi,Ogasawara, Kunio

, p. 1779 - 1788 (2007/10/02)

The allyl trichloroacetates, (6) and (7), have been converted into the trichloro-γ-lactones, (8) and (9), by cuprous chloride.On dechlorination using tri-n-butyltin hydride, regioselective reaction has occurred initially at α position to convert the trich

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