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CAS

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86776-07-0

4-(2,6-Dimethyl-pyridin-4-ylamino)-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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  • 86776-07-0 Structure

  • Basic information

    1. Product Name: 4-(2,6-Dimethyl-pyridin-4-ylamino)-benzoic acid
    2. Synonyms: 4-(2,6-Dimethyl-pyridin-4-ylamino)-benzoic acid
    3. CAS NO:86776-07-0
    4. Molecular Formula:
    5. Molecular Weight: 242.277
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 86776-07-0.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: 4-(2,6-Dimethyl-pyridin-4-ylamino)-benzoic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(2,6-Dimethyl-pyridin-4-ylamino)-benzoic acid(86776-07-0)
    11. EPA Substance Registry System: 4-(2,6-Dimethyl-pyridin-4-ylamino)-benzoic acid(86776-07-0)

  • 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: 86776-07-0(Hazardous Substances Data)

86776-07-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86776-07-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,7,7 and 6 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 86776-07:
(7*8)+(6*6)+(5*7)+(4*7)+(3*6)+(2*0)+(1*7)=180
180 % 10 = 0
So 86776-07-0 is a valid CAS Registry Number.

86776-07-0Upstream product

86776-07-0Downstream Products

86776-07-0Relevant articles and documents

Synthetic Applications of N-N Linked Heterocycles. Part 15. A Facile Synthesis of 4-Pyridyl(aryl)amines via the Reaction between 4-Chloro-1-pyridiniopyridinium Salts and Aryl Amines

Sammes, Michael P.,Ho, King-Wah,Tam, Ming-Lim,Katritzky, Alan R.

, p. 973 - 978 (2007/10/02)

4-Chloro-1-pyridiniopyridinium salts (7) and (8) react with primary and secondary arylamines to give high yields of isolable 4-aryliminium salts (9) and (10).These are readily fragmented into 4-pyridyl(aryl)amines (11) and (12) in excellent yields on treatment with sodium cyanide or sodium salts of sulphonic acids.The method fails with the more basic aliphatic amines, since these apparently attack the 2-position of the chloropyridinium ring giving products resulting from ring-opening.Mechanisms of the reactions are discussed.

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