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C16H17N3O2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1010687-47-4 Structure
  • Basic information

    1. Product Name: C16H17N3O2
    2. Synonyms: C16H17N3O2
    3. CAS NO:1010687-47-4
    4. Molecular Formula:
    5. Molecular Weight: 283.33
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1010687-47-4.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: C16H17N3O2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C16H17N3O2(1010687-47-4)
    11. EPA Substance Registry System: C16H17N3O2(1010687-47-4)
  • 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: 1010687-47-4(Hazardous Substances Data)

1010687-47-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1010687-47-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,0,6,8 and 7 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1010687-47:
(9*1)+(8*0)+(7*1)+(6*0)+(5*6)+(4*8)+(3*7)+(2*4)+(1*7)=114
114 % 10 = 4
So 1010687-47-4 is a valid CAS Registry Number.

1010687-47-4Downstream Products

1010687-47-4Relevant articles and documents

Dithiocarbamate and CuO promoted one-pot synthesis of 2-(N-substituted)-aminobenzimidazoles and related heterocycles

Das, Parthasarathi,Kumar, C. Kiran,Kumar, K. Naresh,Innus,Iqbal, Javed,Srinivas, Nanduri

, p. 992 - 995 (2008/09/17)

A rapid and efficient one-pot method for the synthesis of 2-(N-substituted)-aminobenzimidazoles is described. The reaction is promoted by dithiocarbamate and catalytic CuO. This procedure is general and can be applied to synthesize many potential drug can

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