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CAS

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1313762-34-3

N-(3,6-diMethylpyridin-2-yl)pivalaMide, with the molecular formula C13H19N3O, is an amide derivative of pivalic acid featuring a pyridine ring with two methyl groups at the 3 and 6 positions. This chemical compound is known for its unique structure and reactivity, making it a valuable tool in the development of new chemical entities and materials.

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  • 1313762-34-3 Structure

  • Basic information

    1. Product Name: N-(3,6-diMethylpyridin-2-yl)pivalaMide
    2. Synonyms: N-(3,6-diMethylpyridin-2-yl)pivalaMide
    3. CAS NO:1313762-34-3
    4. Molecular Formula: C12H18N2O
    5. Molecular Weight: 206.28412
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1313762-34-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 337.7±37.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.042±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 13.83±0.70(Predicted)
    10. CAS DataBase Reference: N-(3,6-diMethylpyridin-2-yl)pivalaMide(CAS DataBase Reference)
    11. NIST Chemistry Reference: N-(3,6-diMethylpyridin-2-yl)pivalaMide(1313762-34-3)
    12. EPA Substance Registry System: N-(3,6-diMethylpyridin-2-yl)pivalaMide(1313762-34-3)

  • 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: 1313762-34-3(Hazardous Substances Data)

1313762-34-3 Usage

Uses

Used in Organic Synthesis:
N-(3,6-diMethylpyridin-2-yl)pivalaMide is used as a reagent in organic synthesis for the preparation of various heterocyclic compounds. Its distinctive structure allows for the creation of a wide range of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, N-(3,6-diMethylpyridin-2-yl)pivalaMide serves as a building block for the synthesis of potential drug candidates. Its unique properties and reactivity contribute to the development of innovative medications and therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 1313762-34-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,3,7,6 and 2 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1313762-34:
(9*1)+(8*3)+(7*1)+(6*3)+(5*7)+(4*6)+(3*2)+(2*3)+(1*4)=133
133 % 10 = 3
So 1313762-34-3 is a valid CAS Registry Number.

1313762-34-3Relevant articles and documents

Inter- and intramolecular hydroacylation of alkenes employing a bifunctional catalyst system

Vautravers, Nicolas R.,Regent, Damien D.,Breit, Bernhard

supporting information; experimental part, p. 6635 - 6637 (2011/06/27)

Based on a conceptually innovative bifunctional P,N ligand, an efficient protocol for the rhodium-catalyzed inter- and intramolecular hydroacylation of alkenes has been developed.

Discovery of [3-(4,5,7-trifluoro-benzothiazol-2-ylmethyl)-pyrrolo[2,3-b]pyridin-1-yl] acetic acids as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications

Van Zandt, Michael C.,Doan, Brian,Sawicki, Diane R.,Sredy, Janet,Podjarny, Alberto D.

supporting information; experimental part, p. 2006 - 2008 (2009/11/30)

Efforts to identify treatments for chronic diabetic complications have resulted in the discovery of a novel series of highly potent and selective [3-(4,5,7-trifluoro-benzothiazol-2-ylmethyl)-pyrrolo[2,3-b]pyridin-1-yl] acetic acid aldose reductase inhibitors. The lead candidate, [6-methyl-3-(4,5,7-trifluoro-benzothiazol-2-ylmethyl)-pyrrolo[2,3-b]pyri din-1-yl]acetic acid example 16, inhibits aldose reductase with an IC50 of 8 nM, while being inactive against aldehyde reductase (IC50 > 100 μM), a related enzyme involved in the detoxification of reactive aldehydes.

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