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CAS

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176983-04-3

2-Ethylsulfanylmethyl-benzonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 176983-04-3 Structure

  • Basic information

    1. Product Name: 2-Ethylsulfanylmethyl-benzonitrile
    2. Synonyms: 2-Ethylsulfanylmethyl-benzonitrile
    3. CAS NO:176983-04-3
    4. Molecular Formula:
    5. Molecular Weight: 177.27
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 176983-04-3.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: 2-Ethylsulfanylmethyl-benzonitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Ethylsulfanylmethyl-benzonitrile(176983-04-3)
    11. EPA Substance Registry System: 2-Ethylsulfanylmethyl-benzonitrile(176983-04-3)

  • 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: 176983-04-3(Hazardous Substances Data)

176983-04-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 176983-04-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,6,9,8 and 3 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 176983-04:
(8*1)+(7*7)+(6*6)+(5*9)+(4*8)+(3*3)+(2*0)+(1*4)=183
183 % 10 = 3
So 176983-04-3 is a valid CAS Registry Number.

176983-04-3Relevant articles and documents

Tandem Pummerer-Diels-Alder reaction sequence. A novel cascade process for the preparation of 1-arylnaphthalene lignans

Padwa, Albert,Cochran, John E.,Kappe, C. Oliver

, p. 3706 - 3714 (1996)

The α-thiocarbocation generated from the Pummerer reaction of an o-benzoyl-substituted sulfoxide is intercepted by the adjacent keto group to produce an α-thio isobenzofuran as a transient intermediate which undergoes a subsequent Diels-Alder cycloadditio

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