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164791-48-4

2-tert-butylthio-3-chlorobenzaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 164791-48-4 Structure

  • Basic information

    1. Product Name: 2-tert-butylthio-3-chlorobenzaldehyde
    2. Synonyms: 2-tert-butylthio-3-chlorobenzaldehyde
    3. CAS NO:164791-48-4
    4. Molecular Formula:
    5. Molecular Weight: 228.743
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 164791-48-4.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-tert-butylthio-3-chlorobenzaldehyde(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-tert-butylthio-3-chlorobenzaldehyde(164791-48-4)
    11. EPA Substance Registry System: 2-tert-butylthio-3-chlorobenzaldehyde(164791-48-4)

  • 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: 164791-48-4(Hazardous Substances Data)

164791-48-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 164791-48-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,4,7,9 and 1 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 164791-48:
(8*1)+(7*6)+(6*4)+(5*7)+(4*9)+(3*1)+(2*4)+(1*8)=164
164 % 10 = 4
So 164791-48-4 is a valid CAS Registry Number.

164791-48-4Downstream Products

164791-48-4Relevant articles and documents

One-pot synthesis of 2H-thiochromenes via TiCl4-promoted reaction of 2-tert-butylthiobenzaldehydes with activated alkenes

Chang, Hoon Lee,Lee, Kee-Jung

experimental part, p. 1023 - 1027 (2009/12/06)

(Chemical Equation Presented) A facile synthesis of 2H-thiochromenes through TiCl4-promoted reaction of 2-tert-butylthiobenzaldehydes with activated alkenes is described.

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