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CAS

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1253765-35-3

N-allyl-2-(hex-1-ynylthio)-5-nitrobenzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1253765-35-3 Structure

  • Basic information

    1. Product Name: N-allyl-2-(hex-1-ynylthio)-5-nitrobenzamide
    2. Synonyms: N-allyl-2-(hex-1-ynylthio)-5-nitrobenzamide
    3. CAS NO:1253765-35-3
    4. Molecular Formula:
    5. Molecular Weight: 318.397
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1253765-35-3.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: N-allyl-2-(hex-1-ynylthio)-5-nitrobenzamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-allyl-2-(hex-1-ynylthio)-5-nitrobenzamide(1253765-35-3)
    11. EPA Substance Registry System: N-allyl-2-(hex-1-ynylthio)-5-nitrobenzamide(1253765-35-3)

  • 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: 1253765-35-3(Hazardous Substances Data)

1253765-35-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1253765-35-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,3,7,6 and 5 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1253765-35:
(9*1)+(8*2)+(7*5)+(6*3)+(5*7)+(4*6)+(3*5)+(2*3)+(1*5)=163
163 % 10 = 3
So 1253765-35-3 is a valid CAS Registry Number.

1253765-35-3Downstream Products

1253765-35-3Relevant articles and documents

Cu and Ag catalyzed oxidative arylthiation of terminal acetylenes

Henke, Adam,Srogl, Jiri

supporting information; experimental part, p. 6819 - 6821 (2010/10/20)

A mild Cu or Ag catalyzed oxidative arylthiation of terminal acetylenes is introduced. The process, featuring metal catalyzed C-H bond activation as a key step, leads to the formation of highly substituted mercaptoacetylenes under unprecedented neutral conditions.

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