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1262034-99-0

C38H22Cl4S4 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1262034-99-0 Structure

  • Basic information

    1. Product Name: C38H22Cl4S4
    2. Synonyms: C38H22Cl4S4
    3. CAS NO:1262034-99-0
    4. Molecular Formula:
    5. Molecular Weight: 748.669
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1262034-99-0.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: C38H22Cl4S4(CAS DataBase Reference)
    10. NIST Chemistry Reference: C38H22Cl4S4(1262034-99-0)
    11. EPA Substance Registry System: C38H22Cl4S4(1262034-99-0)

  • 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: 1262034-99-0(Hazardous Substances Data)

1262034-99-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1262034-99-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,2,0,3 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1262034-99:
(9*1)+(8*2)+(7*6)+(6*2)+(5*0)+(4*3)+(3*4)+(2*9)+(1*9)=130
130 % 10 = 0
So 1262034-99-0 is a valid CAS Registry Number.

1262034-99-0Downstream Products

1262034-99-0Relevant articles and documents

Mild persubstitution of di- and tetrabrominated arenes with arylthiolate nucleophiles

Del Rosso, Pablo G.,Almassio, Marcela F.,Bruno, Mattia,Garay, Raúl O.

, p. 6730 - 6733 (2010)

A mild selective protocol was used to prepare tetrakis(2-chlorophenylthio) anthracene from tetrabromoanthracene and sodium 2-chlorobenzenethiolate avoiding the thiolate self-attack. The uncatalyzed nucleophilic substitution of a series of mono-, di-, and tetrabrominated arenes by arylthiolate ions was attempted in mild conditions to investigate the scope of the substitution reaction regarding the size of the aromatic system as well as the number of bromine atoms. Successful reactions afforded only the persubstituted products in good purity and yield after a simple workup and chemoselectivity of Br versus Cl substituents was achieved for the tetrabromide.

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