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C17H17NO4 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1146220-53-2 Structure
  • Basic information

    1. Product Name: C17H17NO4
    2. Synonyms: C17H17NO4
    3. CAS NO:1146220-53-2
    4. Molecular Formula:
    5. Molecular Weight: 299.326
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1146220-53-2.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: C17H17NO4(CAS DataBase Reference)
    10. NIST Chemistry Reference: C17H17NO4(1146220-53-2)
    11. EPA Substance Registry System: C17H17NO4(1146220-53-2)
  • 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: 1146220-53-2(Hazardous Substances Data)

1146220-53-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1146220-53-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,6,2,2 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1146220-53:
(9*1)+(8*1)+(7*4)+(6*6)+(5*2)+(4*2)+(3*0)+(2*5)+(1*3)=112
112 % 10 = 2
So 1146220-53-2 is a valid CAS Registry Number.

1146220-53-2Downstream Products

1146220-53-2Relevant articles and documents

Simple synthesis of 3-acetamido-β-resorcylic acids as potential FabF and FabH inhibitors without using protecting groups

Mara?, Nenad,Anderluh, Petra ?tefani?,Urleb, Uro?,Ko?evar, Marijan

experimental part, p. 437 - 440 (2009/07/25)

A simple two-step strategy for the synthesis of 3-acetamido-β- resorcylic acids as potential platensimycin analogues was developed. It avoids the use of protecting group chemistry and starts from 2-aminoresorcinol, which is first N-acylated and then subje

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