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3,4-dimethoxy-2-(methylthio)benzoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1089199-05-2 Structure
  • Basic information

    1. Product Name: 3,4-dimethoxy-2-(methylthio)benzoic acid
    2. Synonyms: 3,4-dimethoxy-2-(methylthio)benzoic acid
    3. CAS NO:1089199-05-2
    4. Molecular Formula:
    5. Molecular Weight: 228.269
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1089199-05-2.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: 3,4-dimethoxy-2-(methylthio)benzoic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,4-dimethoxy-2-(methylthio)benzoic acid(1089199-05-2)
    11. EPA Substance Registry System: 3,4-dimethoxy-2-(methylthio)benzoic acid(1089199-05-2)
  • 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: 1089199-05-2(Hazardous Substances Data)

1089199-05-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1089199-05-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,8,9,1,9 and 9 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1089199-05:
(9*1)+(8*0)+(7*8)+(6*9)+(5*1)+(4*9)+(3*9)+(2*0)+(1*5)=192
192 % 10 = 2
So 1089199-05-2 is a valid CAS Registry Number.

1089199-05-2Downstream Products

1089199-05-2Relevant articles and documents

Competition of substituents for ortho direction of metalation of veratric acid

Chau, Nguyet Trang Thanh,Nguyen, Thi Huu,Castanet, Anne-Sophie,Nguyen, Kim Phi Phung,Mortier, Jacques

, p. 10552 - 10557 (2008)

LTMP (5 equiv) metalates randomly veratric acid (1). Under external quench conditions, the thermodynamically more stable lithium 2-lithio-3,4-dimethoxybenzoate (2) reacts with a variety of electrophiles to give versatile building units that are not easily accessible by conventional means. Under in situ quench conditions (LTMP/TMSCl), a reversal of regioselectivity is observed and 6-trimethylsilyl-3,4-dimethoxybenzoic acid (10) is formed predominantly.

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