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74420-04-5

1-Benzyl-4-Chloro-1H-pyrrolo<2,3-b>pyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 74420-04-5 Structure

  • Basic information

    1. Product Name: 1-Benzyl-4-Chloro-1H-pyrrolo<2,3-b>pyridine
    2. Synonyms: 1-Benzyl-4-Chloro-1H-pyrrolo<2,3-b>pyridine
    3. CAS NO:74420-04-5
    4. Molecular Formula:
    5. Molecular Weight: 242.708
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 74420-04-5.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: 1-Benzyl-4-Chloro-1H-pyrrolo<2,3-b>pyridine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-Benzyl-4-Chloro-1H-pyrrolo<2,3-b>pyridine(74420-04-5)
    11. EPA Substance Registry System: 1-Benzyl-4-Chloro-1H-pyrrolo<2,3-b>pyridine(74420-04-5)

  • 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: 74420-04-5(Hazardous Substances Data)

74420-04-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74420-04-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,4,2 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 74420-04:
(7*7)+(6*4)+(5*4)+(4*2)+(3*0)+(2*0)+(1*4)=105
105 % 10 = 5
So 74420-04-5 is a valid CAS Registry Number.

74420-04-5Downstream Products

74420-04-5Relevant articles and documents

Synthesis of 4-Amino-1H-pyrrolopyridine (1,7-Dideazaadenine) and 1H-Pyrrolopyridin-4-ol (1,7-Dideazahypoxanthine)

Schneller, Stewart W.,Luo, Jiann-Kuan

, p. 4045 - 4048 (2007/10/02)

4-Amino-1H-pyrrolopyridine (1,7-dideazaadenine) (5) has been synthesized by the iron and acetic acid reduction of 4-nitro-1H-pyrrolopyridine 7-oxide (13), obtained by nitration of 1H-pyrrolopyridine-3-carboxamide 7-oxide (17).Other nitration reactions in the 1H-pyrrolopyridine 7-oxide series are disclosed.The preparation of 1H-pyrrolopyridin-4-ol (1,7-dideazahypoxanthine) (6) began with the hydrolysis of ethyl 1-benzyl-3-cyano-4-oxo-4,7-dihydro-1H-pyrrolopyridine-5-carboxylate (21) to the 3,5-dicarboxylic acid derivative of 1-benzyl-4-oxo-4,7-dihydro-1H-pyrrolopyridine (22).Decarboxylation of 22 with subsequent debenzylation formed 6.

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