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Butanoic acid, 4-(4-methyl-2-nitrophenoxy)-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 874210-51-2 Structure
  • Basic information

    1. Product Name: Butanoic acid, 4-(4-methyl-2-nitrophenoxy)-, ethyl ester
    2. Synonyms:
    3. CAS NO:874210-51-2
    4. Molecular Formula: C13H17NO5
    5. Molecular Weight: 267.282
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 874210-51-2.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: Butanoic acid, 4-(4-methyl-2-nitrophenoxy)-, ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Butanoic acid, 4-(4-methyl-2-nitrophenoxy)-, ethyl ester(874210-51-2)
    11. EPA Substance Registry System: Butanoic acid, 4-(4-methyl-2-nitrophenoxy)-, ethyl ester(874210-51-2)
  • 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: 874210-51-2(Hazardous Substances Data)

874210-51-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 874210-51-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,4,2,1 and 0 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 874210-51:
(8*8)+(7*7)+(6*4)+(5*2)+(4*1)+(3*0)+(2*5)+(1*1)=162
162 % 10 = 2
So 874210-51-2 is a valid CAS Registry Number.

874210-51-2Relevant articles and documents

Synthesis of crescent aromatic oligoamides

Yuan, Lihua,Sanford, Adam R.,Feng, Wen,Zhang, Aimin,Zhu, Jin,Zeng, Huaqiang,Yamato, Kazuhiro,Li, Minfeng,Ferguson, Joseph S.,Gong, Bing

, p. 10660 - 10669 (2005)

This article describes the synthetic procedures for the preparation of crescent (and helical) aromatic oligoamides developed in recent years in our laboratory. The large-scale preparation of a variety of monomers derived from various tetrasubstituted benzenes is presented. Three different strategies for constructing various oligomers consisting of meta- and meta/para-linked benzene residues are discussed. Factors affecting coupling efficiency and yields are analyzed. The developed synthetic methods have provided the basis for the preparation of longer oligomers and for the development of solid-phase synthesis.

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