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957470-94-9

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

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  • 957470-94-9 Structure

  • Basic information

    1. Product Name: 4-ethynylbenzamidoxime
    2. Synonyms: 4-ethynylbenzamidoxime
    3. CAS NO:957470-94-9
    4. Molecular Formula:
    5. Molecular Weight: 160.175
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 957470-94-9.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: 4-ethynylbenzamidoxime(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-ethynylbenzamidoxime(957470-94-9)
    11. EPA Substance Registry System: 4-ethynylbenzamidoxime(957470-94-9)

  • 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: 957470-94-9(Hazardous Substances Data)

957470-94-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 957470-94-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,7,4,7 and 0 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 957470-94:
(8*9)+(7*5)+(6*7)+(5*4)+(4*7)+(3*0)+(2*9)+(1*4)=219
219 % 10 = 9
So 957470-94-9 is a valid CAS Registry Number.

957470-94-9Upstream product

957470-94-9Relevant articles and documents

Synthesis, mechanism of formation, and molecular orbital calculations of arylamidoximes

Srivastava, Rajendra M.,Pereira, Maria C.,Faustino, Wagner W. M.,Coutinho, Kaline,Dos Anjos, Janaina V.,De Melo, Sebastiao J.

, p. 1319 - 1324 (2009)

A simple and easy synthesis of ten arylamidoximes from arylnitriles and hydroxylamine is described. The formation of the arylamides has been observed to a much lesser extent in the present work. A new mechanism for the formation of arylamidoximes, as well

Design and synthesis of 3,5-disubstituted boron-containing 1,2,4-oxadiazoles as potential combretastatin A-4 (CA-4) analogs

Das, Bhaskar C.,Tang, Xiang-Ying,Rogler, Patrick,Evans, Todd

supporting information; experimental part, p. 3947 - 3950 (2012/08/14)

We have designed and synthesized a small library of 3,5-disubstituted-1,2, 4-oxadiazole containing combretastatin A-4 (CA-4) analogs. Our objective is to increase the efficacy of the CA-4 as an anti-tubulin and antimitotic agent by substituting the cis-al

Synthesis of glycosyl-triazole linked 1,2,4-oxadiazoles

dos Anjos, Janaina V.,Sinou, Denis,de Melo, Sebastiao J.,Srivastava, Rajendra M.

, p. 2440 - 2449 (2008/02/12)

The synthesis of four different types of oxadiazoles containing a terminal acetylenic group is described. Reaction of these oxadiazoles with various azidoglycosides via a copper-catalyzed [3+2] cycloaddition ('click chemistry') afforded the corresponding

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