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616863-07-1

methyl 2-(naphthalen-2-yloxy)ethyl sulfide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 616863-07-1 Structure

  • Basic information

    1. Product Name: methyl 2-(naphthalen-2-yloxy)ethyl sulfide
    2. Synonyms: methyl 2-(naphthalen-2-yloxy)ethyl sulfide
    3. CAS NO:616863-07-1
    4. Molecular Formula:
    5. Molecular Weight: 218.32
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 616863-07-1.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: methyl 2-(naphthalen-2-yloxy)ethyl sulfide(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 2-(naphthalen-2-yloxy)ethyl sulfide(616863-07-1)
    11. EPA Substance Registry System: methyl 2-(naphthalen-2-yloxy)ethyl sulfide(616863-07-1)

  • 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: 616863-07-1(Hazardous Substances Data)

616863-07-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 616863-07-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,1,6,8,6 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 616863-07:
(8*6)+(7*1)+(6*6)+(5*8)+(4*6)+(3*3)+(2*0)+(1*7)=171
171 % 10 = 1
So 616863-07-1 is a valid CAS Registry Number.

616863-07-1Downstream Products

616863-07-1Relevant articles and documents

Behaviour of iprit carbonate analogues in solventless reactions

Arico',Evaristo,Tundo

, p. 31071 - 31078 (2014)

Sulfur iprit carbonate analogues have been investigated in neat conditions at atmospheric pressure, in the presence and in the absence of a catalytic amount of base. Furthermore, their reaction mechanism has been discussed in detail. In these novel reaction conditions, sulfur mustard carbonate analogues, that previously showed poor or no reactivity, remarkably undergo efficient nucleophilic substitution with several substrates. This journal is the Partner Organisations 2014.

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