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CAS

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334708-19-9

benzyl 2-iodo-5-methoxyphenyl sulfide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 334708-19-9 Structure

  • Basic information

    1. Product Name: benzyl 2-iodo-5-methoxyphenyl sulfide
    2. Synonyms: benzyl 2-iodo-5-methoxyphenyl sulfide
    3. CAS NO:334708-19-9
    4. Molecular Formula:
    5. Molecular Weight: 356.227
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 334708-19-9.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: benzyl 2-iodo-5-methoxyphenyl sulfide(CAS DataBase Reference)
    10. NIST Chemistry Reference: benzyl 2-iodo-5-methoxyphenyl sulfide(334708-19-9)
    11. EPA Substance Registry System: benzyl 2-iodo-5-methoxyphenyl sulfide(334708-19-9)

  • 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: 334708-19-9(Hazardous Substances Data)

334708-19-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 334708-19-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,4,7,0 and 8 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 334708-19:
(8*3)+(7*3)+(6*4)+(5*7)+(4*0)+(3*8)+(2*1)+(1*9)=139
139 % 10 = 9
So 334708-19-9 is a valid CAS Registry Number.

334708-19-9Relevant articles and documents

A novel palladium-mediated coupling approach to 2,3-disubstituted benzo[b]thiophenes and its application to the synthesis of tubulin binding agents

Flynn, Bernard L.,Verdier-Pinard, Pascal,Hamel, Ernest

, p. 651 - 653 (2007/10/03)

Flexible, convergent access to 2,3-disubstituted benzo[b]thiophenes has been developed. The most concise approach involves sequential coupling of o-bromoiodobenzenes with benzylmercaptan and zinc acetylides to give benzyl o-ethynylpnenyl sulfides which re

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