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262436-40-8

4-chloro-N-(2,5-dimethoxyphenyl)benzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 262436-40-8 Structure

  • Basic information

    1. Product Name: 4-chloro-N-(2,5-dimethoxyphenyl)benzamide
    2. Synonyms: 4-chloro-N-(2,5-dimethoxyphenyl)benzamide
    3. CAS NO:262436-40-8
    4. Molecular Formula: C15H14ClNO3
    5. Molecular Weight: 291.72956
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 262436-40-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-chloro-N-(2,5-dimethoxyphenyl)benzamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-chloro-N-(2,5-dimethoxyphenyl)benzamide(262436-40-8)
    11. EPA Substance Registry System: 4-chloro-N-(2,5-dimethoxyphenyl)benzamide(262436-40-8)

  • 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: 262436-40-8(Hazardous Substances Data)

262436-40-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 262436-40-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,2,4,3 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 262436-40:
(8*2)+(7*6)+(6*2)+(5*4)+(4*3)+(3*6)+(2*4)+(1*0)=128
128 % 10 = 8
So 262436-40-8 is a valid CAS Registry Number.

262436-40-8Relevant articles and documents

Thermally induced cyclization of electron-rich N-arylthiobenzamides to benzothiazoles

Barrett, Oscene V.,Downer-Riley, Nadale K.,Jackson, Yvette A.

experimental part, p. 2579 - 2586 (2012/09/07)

Heating N-(2-methoxyphenyl)benzenecarbothioamides in refluxing nitrobenzene for 24 hours gives the corresponding benzothiazoles with intramolecular ipso substitution of the ortho-methoxy substituent. The thermal cyclization of various other N-arylthiobenzamides is also explored. Georg Thieme Verlag Stuttgart · New York.

Reactions of some N-(2,5-dimethoxyaryl)thiobenzamides: En route to an analogue of kuanoniamine A

Jackson, Yvette A.,Lyon, Michael A.,Townsend, Norman,Bellabe, Kettyna,Soltanik, Fernando

, p. 205 - 210 (2007/10/03)

The reactions of some N-(2,5-dimethoxyaryl) thiobenzamides were studied. It was found that nitration of 2-aryl-4,7-dimethoxybenzothiazoles produced a mixture of 5- and 6-nitrobenzothiazoles which were distinguished by synthesis of the 2-aryl-4,7-dimethoxy-6-nitrobenzothiaoles by oxidative cyclization of the corresponding nitrothiobenzanilides. The results showed that the cyclization of arylthioanilides was influenced by the nature of the ring substituents.

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