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C22H20ClN3O2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1649461-04-0 Structure
  • Basic information

    1. Product Name: C22H20ClN3O2
    2. Synonyms: C22H20ClN3O2
    3. CAS NO:1649461-04-0
    4. Molecular Formula:
    5. Molecular Weight: 393.873
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1649461-04-0.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: C22H20ClN3O2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C22H20ClN3O2(1649461-04-0)
    11. EPA Substance Registry System: C22H20ClN3O2(1649461-04-0)
  • 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: 1649461-04-0(Hazardous Substances Data)

1649461-04-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1649461-04-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,4,9,4,6 and 1 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1649461-04:
(9*1)+(8*6)+(7*4)+(6*9)+(5*4)+(4*6)+(3*1)+(2*0)+(1*4)=190
190 % 10 = 0
So 1649461-04-0 is a valid CAS Registry Number.

1649461-04-0Downstream Products

1649461-04-0Relevant articles and documents

Synthesis of 5,7-disubstituted 7H-pyrrolo[2,3-d]pyrimidin-4(3H)-ones and their N-alkylation's under phase transfer conditions

Dave, Chaitanya G.,Patel, Killol J.

, p. 943 - 947 (2014/08/05)

5,7-disubstituted 7H-pyrrolo[2,3-d]pyrimidin-4(3H)-ones 2 were synthesized by the cyclocondensation of 1,4-disubstituted 2-amino-3-cyanopyrrole 1 with formic acid. When comparative study of N versus O alkylation of ambident 5,7-disubstituted 7H-pyrrolo[2,3-d]pyrimidin-4(3H)-ones 2 was carried out under liquid-liquid PTC, solid-liquid PTC, and solid-liquid solvent free conditions using various alkylating agents 3, the N-alkylated product 4 were obtained selectively and exclusively.

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