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632330-04-2

Benzoic acid, 6-acetyl-2,3-dimethoxy-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 632330-04-2 Structure

  • Basic information

    1. Product Name: Benzoic acid, 6-acetyl-2,3-dimethoxy-, methyl ester
    2. Synonyms:
    3. CAS NO:632330-04-2
    4. Molecular Formula: C12H14O5
    5. Molecular Weight: 238.24
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 632330-04-2.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: Benzoic acid, 6-acetyl-2,3-dimethoxy-, methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzoic acid, 6-acetyl-2,3-dimethoxy-, methyl ester(632330-04-2)
    11. EPA Substance Registry System: Benzoic acid, 6-acetyl-2,3-dimethoxy-, methyl ester(632330-04-2)

  • 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: 632330-04-2(Hazardous Substances Data)

632330-04-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 632330-04-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,2,3,3 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 632330-04:
(8*6)+(7*3)+(6*2)+(5*3)+(4*3)+(3*0)+(2*0)+(1*4)=112
112 % 10 = 2
So 632330-04-2 is a valid CAS Registry Number.

632330-04-2Upstream product

632330-04-2Downstream Products

632330-04-2Relevant articles and documents

Intramolecular Heck reaction of methylenephthalimidine derivatives: A simple route to lennoxamine and chilenine

Kim, Guncheol,Kim, Jin Hee,Kim, Won-Jeong,Kim, Yeon Ah

, p. 8207 - 8209 (2003)

A new concise route to the key intermediate for isoindolobenazepine alkaloids, lennoxamine and chilenine, was developed using amine and keto-ester condensation followed by Heck reaction.

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