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CAS

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193605-64-0

Furo[3,2-c]pyridine-6-carbonitrile, 2,3-dihydro- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 193605-64-0 Structure

  • Basic information

    1. Product Name: Furo[3,2-c]pyridine-6-carbonitrile, 2,3-dihydro- (9CI)
    2. Synonyms: Furo[3,2-c]pyridine-6-carbonitrile, 2,3-dihydro- (9CI)
    3. CAS NO:193605-64-0
    4. Molecular Formula: C8H6N2O
    5. Molecular Weight: 146.14604
    6. EINECS: N/A
    7. Product Categories: PYRIDINE
    8. Mol File: 193605-64-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 303.5±42.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.29±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 1.33±0.20(Predicted)
    10. CAS DataBase Reference: Furo[3,2-c]pyridine-6-carbonitrile, 2,3-dihydro- (9CI)(CAS DataBase Reference)
    11. NIST Chemistry Reference: Furo[3,2-c]pyridine-6-carbonitrile, 2,3-dihydro- (9CI)(193605-64-0)
    12. EPA Substance Registry System: Furo[3,2-c]pyridine-6-carbonitrile, 2,3-dihydro- (9CI)(193605-64-0)

  • 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: 193605-64-0(Hazardous Substances Data)

193605-64-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 193605-64-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,3,6,0 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 193605-64:
(8*1)+(7*9)+(6*3)+(5*6)+(4*0)+(3*5)+(2*6)+(1*4)=150
150 % 10 = 0
So 193605-64-0 is a valid CAS Registry Number.

193605-64-0Downstream Products

193605-64-0Relevant articles and documents

Furopyridines. XXIV [1]. Nitration, Chlorination, Acetoxylation and Cyanation of 2,3-Dihydrofuro[2,3-b]-, -[3,2-b]-, -[2,3-c]- and -[3,2-c]pyridine N-Oxides

Shiotani, Shunsaku,Kurosaki, Masahide,Taniguchi, Katsunori,Moriyama, Miwa

, p. 941 - 952 (2007/10/03)

Nitration of 2,3-dihydrofuro[3,2-b]- N-oxide 3b and -[2,3-c] pyridine N-oxide 3c afforded the nitropyridine compounds 4b, 5b and 6 from 3b and 4c, 5c, 5′c and 7 from 3c, while -[2,3-b]- N-oxide 3a and -[3,2-c]pyridine N-oxide 3d did not give the nitro compound. Chlorination of 3b and 3c with phosphorus oxychloride yielded mainly the chloropyridine derivatives 15b, 15′b from 3b and 15c and 15′c from 3c, whereas 3a and 3d gave pyridine derivatives formed through fission of the 1-2 ether bond of the furopyridines 13a, 14 and 13d. Acetoxylation of 3b and 3c gave 3-acetoxy derivatives 18b and 18c and the parent compound 1b and 1c. Acetoxylation of 3a yielded compounds formed through fission of the 1-2 bond 16 and 17 and 3d gave furopyridones 19 and 19′. Cyanation of 3b and 3c yielded mainly the cyanopyridine compounds 20b, 20c and 20′c. Cyanation of 3a and 3d gave the cyanopyridine compounds 20a, 20d and 20′d accompanying formation of the pyridine derivatives 21a, 21d and 21′d.

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