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1035869-07-8

C8H7ClOS is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1035869-07-8 Structure

  • Basic information

    1. Product Name: C8H7ClOS
    2. Synonyms: C8H7ClOS
    3. CAS NO:1035869-07-8
    4. Molecular Formula:
    5. Molecular Weight: 186.662
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1035869-07-8.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: C8H7ClOS(CAS DataBase Reference)
    10. NIST Chemistry Reference: C8H7ClOS(1035869-07-8)
    11. EPA Substance Registry System: C8H7ClOS(1035869-07-8)

  • 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: 1035869-07-8(Hazardous Substances Data)

1035869-07-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1035869-07-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,5,8,6 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1035869-07:
(9*1)+(8*0)+(7*3)+(6*5)+(5*8)+(4*6)+(3*9)+(2*0)+(1*7)=158
158 % 10 = 8
So 1035869-07-8 is a valid CAS Registry Number.

1035869-07-8Upstream product

1035869-07-8Downstream Products

1035869-07-8Relevant articles and documents

Facile Synthesis of 2,5-Disubstituted Thiazoles from Terminal Alkynes, Sulfonyl Azides, and Thionoesters

Miura, Tomoya,Funakoshi, Yuuta,Fujimoto, Yoshikazu,Nakahashi, Junki,Murakami, Masahiro

, p. 2454 - 2457 (2015)

A sequential procedure for the synthesis of 2,5-disubstituted thiazoles from terminal alkynes, sulfonyl azides, and thionoesters is reported. A copper(I)-catalyzed 1,3-dipolar cycloaddition of terminal alkynes with sulfonyl azides affords 1-sulfonyl-1,2,3-triazoles, which then react with thionoesters in the presence of a rhodium(II) catalyst. The resulting 3-sulfonyl-4-thiazolines subsequently aromatize into the corresponding 2,5-disubstituted thiazoles by elimination of the sulfonyl group. (Chemical Equation Presented).

2,4-Disubstituted-5-acetoxythiazoles: useful intermediates for the synthesis of thiazolones and 2,4,5-trisubstituted thiazoles

Qiao,Dominique,Goodnow Jr.

, p. 3682 - 3686 (2008/09/20)

A variety of 2,4-disubstituted-5-acetoxythiazoles were prepared from the substituted methyl benzoates in good to moderate yields using a three-step sequence: (1) ester to thionoester conversion, (2) coupling with an amino acid, and (3) acetic anhydride me

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