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2-Acetyl-5-methoxy-benzoic acid ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 132338-35-3 Structure
  • Basic information

    1. Product Name: 2-Acetyl-5-methoxy-benzoic acid ethyl ester
    2. Synonyms: 2-Acetyl-5-methoxy-benzoic acid ethyl ester
    3. CAS NO:132338-35-3
    4. Molecular Formula:
    5. Molecular Weight: 222.241
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 132338-35-3.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-Acetyl-5-methoxy-benzoic acid ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Acetyl-5-methoxy-benzoic acid ethyl ester(132338-35-3)
    11. EPA Substance Registry System: 2-Acetyl-5-methoxy-benzoic acid ethyl ester(132338-35-3)
  • 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: 132338-35-3(Hazardous Substances Data)

132338-35-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132338-35-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,3,3 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 132338-35:
(8*1)+(7*3)+(6*2)+(5*3)+(4*3)+(3*8)+(2*3)+(1*5)=103
103 % 10 = 3
So 132338-35-3 is a valid CAS Registry Number.

132338-35-3Relevant articles and documents

A facile synthetic method of herbicidal 2,-dihydro-3-methylene-2-substituted - phenyl-1hisoindol-1-one derivatives

Kim, Jae Nyoung,Ryu, Eung K.

, p. 67 - 74 (2007/10/03)

Herbicidal 2,3-dihydro-3-methylene-2-substitutedphenyl-1 H-isoindol-1-one derivatives 7 have been synthesized. They were prepared from the easily available phenol derivatives 1 in 5 steps in moderate yields.

Synthesis of o-acylarylcarboxylic esters: A new replacement of phenolic hydroxyl by a carbonyl group

Katritzky,Kotali

, p. 6781 - 6784 (2007/10/02)

A wide variety of the title esters are prepared in good yields via a new two step replacement of phenolic hydroxyl by an ethoxycarbonyl group.

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