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Ethanone, 1-(3-pyridinyl)-, O-[(4-methylphenyl)sulfonyl]oxime is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 74209-51-1 Structure
  • Basic information

    1. Product Name: Ethanone, 1-(3-pyridinyl)-, O-[(4-methylphenyl)sulfonyl]oxime
    2. Synonyms: 1-(3-pyridinyl)-ethanone O-[(4-methylphenyl)sulphonyl]-oxime;
    3. CAS NO:74209-51-1
    4. Molecular Formula: C14H14N2O3S
    5. Molecular Weight: 290.343
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 74209-51-1.mol
  • Chemical Properties

    1. Melting Point: 77-79 °C(Solv: ethanol (64-17-5); water (7732-18-5))
    2. Boiling Point: 441.9±47.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: 1.23±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Ethanone, 1-(3-pyridinyl)-, O-[(4-methylphenyl)sulfonyl]oxime(CAS DataBase Reference)
    10. NIST Chemistry Reference: Ethanone, 1-(3-pyridinyl)-, O-[(4-methylphenyl)sulfonyl]oxime(74209-51-1)
    11. EPA Substance Registry System: Ethanone, 1-(3-pyridinyl)-, O-[(4-methylphenyl)sulfonyl]oxime(74209-51-1)
  • 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: 74209-51-1(Hazardous Substances Data)

74209-51-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74209-51-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,2,0 and 9 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 74209-51:
(7*7)+(6*4)+(5*2)+(4*0)+(3*9)+(2*5)+(1*1)=121
121 % 10 = 1
So 74209-51-1 is a valid CAS Registry Number.

74209-51-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-pyridin-3-yl-ethanone oxime O-tosylate

1.2 Other means of identification

Product number -
Other names 1-(3-pyridinyl)-ethanone O-[(4-methylphenyl)sulphonyl]-oxime

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:74209-51-1 SDS

74209-51-1Relevant articles and documents

Synthesis and Antibacterial Activity of Novel 4″-O-desosaminyl clarithromycin derivatives with 11, 12-arylalkyl side chains

Zhao, Zhe-Hui,Zhu, Di,Zhang, Xiao-Xi,Luo, Zhi-Gang,Lei, Ping-Sheng

, p. 1 - 9 (2018/04/24)

A series of novel 4″-O-desosaminyl clarithromycin derivatives with 11, 12-arylalkyl side chains was synthesized by coupling 6-deoxy-desosamine donors (18, 19) with 4″-OH of compounds 5a–c. The activities of the target compounds were tested against a series of macrolide-sensitive and macrolide-resistant pathogens. Some of them showed activities against macrolide sensitive and resistant pathogens, and compounds 21d and 21e displayed significant improvement of activities against resistant pathogens.

PROCESS FOR THE SYNTHESIS OF SUBSTITUTED UREA COMPOUNDS

-

, (2014/02/16)

A process for preparing a substituted urea compound of Formula II or Formula I, or a pharmaceutically acceptable salt or ester thereof, Formula II, Formula I the process comprising the reaction of an intermediate of Formula II' or Formula 1', Formula II',

Efficient synthesis of 2-imidazol-2-ylacetates

Ha, Jae Du,Lee, Su Jung,Nam, So Yeun,Kang, Seung Kyu,Cho, Seung Yoon,Ahn, Jin Hee,Choi, Joong-Kwon

, p. 6201 - 6204 (2007/10/03)

A simple method of synthesizing various 2-imidazol-2-ylacetates is described. Condensation of α-aminoketals with imidates, followed by cyclization in refluxing 4 M-HCl/Dioxane, yielded 2-imidazol-2-ylacetates under one-pot and mild reaction conditions.

Process for preparing pyridine-substituted amino ketal derivatives

-

Page 5, (2008/06/13)

The present invention relates to an efficient process for preparing derivatives of 1-(pyridinyl)-1,1-dialkoxy-2-aminoethane of the formula (I), with which compounds of the formula (I) can be prepared in high purity and yield and in the form of the free ba

Gamma-hydroxy-2-(fluoroalkylaminocarbonyl)-1-piperazinepentanamides and uses thereof

-

Page/Page column 195, (2010/01/31)

γ-Hydroxy-2-(fluoroalkylaminocarbonyl)-1-piperazinepentanamide compounds are inhibitors of HIV protease and inhibitors of HIV replication. These compounds are useful in the prevention or treatment of infection by HV and the treatment of AIDS, either as compounds, pharmaceutically acceptable salts, pharmaceutical composition ingredients, whether or not in combination with other antivirals, immunomodulators, antibiotics or vaccines. Methods of treating AIDS and methods of preventing or treating infection by HIV are also described. These compounds are effective against HIV viral mutants which are resistant to HIV protease inhibitors currently used for treating AIDS and HIV infection.

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