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869892-67-1

3-(1-methoxycarbonyl-ethoxy)-4-methylbenzoic acid 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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  • 869892-67-1 Structure

  • Basic information

    1. Product Name: 3-(1-methoxycarbonyl-ethoxy)-4-methylbenzoic acid methyl ester
    2. Synonyms: 3-(1-methoxycarbonyl-ethoxy)-4-methylbenzoic acid methyl ester
    3. CAS NO:869892-67-1
    4. Molecular Formula:
    5. Molecular Weight: 252.267
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 869892-67-1.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: 3-(1-methoxycarbonyl-ethoxy)-4-methylbenzoic acid methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(1-methoxycarbonyl-ethoxy)-4-methylbenzoic acid methyl ester(869892-67-1)
    11. EPA Substance Registry System: 3-(1-methoxycarbonyl-ethoxy)-4-methylbenzoic acid methyl ester(869892-67-1)

  • 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: 869892-67-1(Hazardous Substances Data)

869892-67-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 869892-67-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,9,8,9 and 2 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 869892-67:
(8*8)+(7*6)+(6*9)+(5*8)+(4*9)+(3*2)+(2*6)+(1*7)=261
261 % 10 = 1
So 869892-67-1 is a valid CAS Registry Number.

869892-67-1Relevant articles and documents

Design and synthesis of aromatic inhibitors of anthranilate synthase

Payne, Richard J.,Bulloch, Esther M.M.,Abell, Andrew D.,Abell, Chris

, p. 3629 - 3635 (2005)

Anthranilate synthase catalyses the conversion of chorismate to anthranilate, a key step in tryptophan biosynthesis. A series of 3-(1-carboxy-ethoxy) benzoic acids were synthesised as chorismate analogues, with varying functionality at C-4, the position of the departing hydroxyl group in chorismate. Most of the compounds were moderate inhibitors of anthranilate synthase, with inhibition constants between 20-30 μM. The exception was 3-(1-carboxy-ethoxy) benzoic acid, (C-4 = H), for which K1 = 2.4 μM. These results suggest that a hydrogen bonding interaction with the active site general acid (Glu309) is less important than previously assumed for inhibition of the enzyme by these aromatic chorismate analogues. The Royal Society of Chemistry 2005.

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