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

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  • 173095-00-6 Structure
  • Basic information

    1. Product Name: 2-(3,4-dimethoxy-phenylamino)-nicotinic acid
    2. Synonyms: 2-(3,4-dimethoxy-phenylamino)-nicotinic acid
    3. CAS NO:173095-00-6
    4. Molecular Formula: C14H14N2O4
    5. Molecular Weight: 274
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 173095-00-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-(3,4-dimethoxy-phenylamino)-nicotinic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(3,4-dimethoxy-phenylamino)-nicotinic acid(173095-00-6)
    11. EPA Substance Registry System: 2-(3,4-dimethoxy-phenylamino)-nicotinic acid(173095-00-6)
  • 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: 173095-00-6(Hazardous Substances Data)

173095-00-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 173095-00-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,3,0,9 and 5 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 173095-00:
(8*1)+(7*7)+(6*3)+(5*0)+(4*9)+(3*5)+(2*0)+(1*0)=126
126 % 10 = 6
So 173095-00-6 is a valid CAS Registry Number.

173095-00-6Downstream Products

173095-00-6Relevant articles and documents

Improvement of the Ullmann's condensation method for the synthesis of 2-anilinonicotinic acids

Misbahi, Houria,Brouant, Pierre,Barbe, Jacques

, p. 335 - 336 (2007/10/03)

Several 2-anilinonicotinic acid derivatives were prepared under the Ullmann's reaction conditions by condensation of 2-chloronicotinic acid and various substituted anilines. Improvement of the procedure based on the effect of the catalyst and that of the

Potential Anticancer Benzo-naphthyridones with Fused Rings: a Theoretical Model for Predicting Orientation in the Cyclization of Intermediates

Mefetah, Hafid,Brouant, Pierre,Galy, Anne-Marie,Galy, Jean-Pierre,Barbe, Jacques

, p. 522 - 533 (2007/10/03)

Synthesis of benzo[b]-1,8-naphthyridine-5-ones with fused ring from halonicotinic acids and amino-substituted benzoheterocycles, leads either to an isomeric mixture or to single isomers. MO calculations conducted on the starting amino-substituted benzoheterocycles, allow predictions of the derivative(s) to be obtained. Some selected compounds belonging to this series were screened in vitro against several human tumor cell lines.

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