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156743-12-3

phenyl (2E,4E) 5-iodo-2,4-pentadienthioate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 156743-12-3 Structure

  • Basic information

    1. Product Name: phenyl (2E,4E) 5-iodo-2,4-pentadienthioate
    2. Synonyms: phenyl (2E,4E) 5-iodo-2,4-pentadienthioate
    3. CAS NO:156743-12-3
    4. Molecular Formula:
    5. Molecular Weight: 316.162
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 156743-12-3.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: phenyl (2E,4E) 5-iodo-2,4-pentadienthioate(CAS DataBase Reference)
    10. NIST Chemistry Reference: phenyl (2E,4E) 5-iodo-2,4-pentadienthioate(156743-12-3)
    11. EPA Substance Registry System: phenyl (2E,4E) 5-iodo-2,4-pentadienthioate(156743-12-3)

  • 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: 156743-12-3(Hazardous Substances Data)

156743-12-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 156743-12-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,7,4 and 3 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 156743-12:
(8*1)+(7*5)+(6*6)+(5*7)+(4*4)+(3*3)+(2*1)+(1*2)=143
143 % 10 = 3
So 156743-12-3 is a valid CAS Registry Number.

156743-12-3Relevant articles and documents

A New Straightforward, and General Approach to Dienamide Natural Products

Babudri, Francesco,Fiandanese, Vito,Naso, Francesco,Punzi, Angela

, p. 2067 - 2070 (1994)

A new synthetic approach to various conjugated (E,E) dienamides has been developed, starting from an easily accessible bifunctional dienyl compound and based upon a double selective electrophilic substitution, followed by coupling reactions.

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