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Benzoic acid, 5-bromo-2-[[4-(methoxycarbonyl)phenoxy]methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 138639-75-5 Structure
  • Basic information

    1. Product Name: Benzoic acid, 5-bromo-2-[[4-(methoxycarbonyl)phenoxy]methyl]-
    2. Synonyms:
    3. CAS NO:138639-75-5
    4. Molecular Formula: C16H13BrO5
    5. Molecular Weight:
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 138639-75-5.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, 5-bromo-2-[[4-(methoxycarbonyl)phenoxy]methyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzoic acid, 5-bromo-2-[[4-(methoxycarbonyl)phenoxy]methyl]-(138639-75-5)
    11. EPA Substance Registry System: Benzoic acid, 5-bromo-2-[[4-(methoxycarbonyl)phenoxy]methyl]-(138639-75-5)
  • 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: 138639-75-5(Hazardous Substances Data)

138639-75-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138639-75-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,6,3 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 138639-75:
(8*1)+(7*3)+(6*8)+(5*6)+(4*3)+(3*9)+(2*7)+(1*5)=165
165 % 10 = 5
So 138639-75-5 is a valid CAS Registry Number.

138639-75-5Downstream Products

138639-75-5Relevant articles and documents

A new series of antiallergic agents. II. Synthesis and activity of new 6,11-dihydrodibenz[b,e]oxepin-carboxylic acid derivatives

Kumazawa,Ohshima,Harakawa,Sato,Obase,Oiji,Ishii,Ishii,Ohmori

, p. 2729 - 2733 (1991)

New methods for the preparation of multi-functionalized-6,11-dihydrodibenz[b,e]oxepins were developed. The structural requirements of KW-4994 (1), a promising orally active antiallergic agent, were defined. A carboxyl group at C-2 was critical for enhanced antiallergic activity of 1. The introduction of bromine atom at C-9 of 1 could elongate the duration of the action of the parent. Antiplatelet activity, a new pharmacological property of this series of compounds, was observed in one of the derivatives of 1.

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