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3-(4-chlorophenyl)-1H-isothiochromen-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 133031-53-5 Structure
  • Basic information

    1. Product Name: 3-(4-chlorophenyl)-1H-isothiochromen-1-one
    2. Synonyms:
    3. CAS NO:133031-53-5
    4. Molecular Formula:
    5. Molecular Weight: 272.755
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 133031-53-5.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: 3-(4-chlorophenyl)-1H-isothiochromen-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(4-chlorophenyl)-1H-isothiochromen-1-one(133031-53-5)
    11. EPA Substance Registry System: 3-(4-chlorophenyl)-1H-isothiochromen-1-one(133031-53-5)
  • 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: 133031-53-5(Hazardous Substances Data)

133031-53-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133031-53-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,0,3 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 133031-53:
(8*1)+(7*3)+(6*3)+(5*0)+(4*3)+(3*1)+(2*5)+(1*3)=75
75 % 10 = 5
So 133031-53-5 is a valid CAS Registry Number.

133031-53-5Downstream Products

133031-53-5Relevant articles and documents

Base-promoted thioannulation of: O -alkynyl oxime ethers with sodium sulfide for the general synthesis of isothiocoumarins

Sun, Cai-Ling,Zhang, Xiao-Hong,Zhang, Xing-Guo,Zhang, Zhu-Zhu

, p. 10174 - 10180 (2021/12/10)

A general and efficient strategy for the one-pot synthesis of isothiocoumarin-1-ones has been developed via the base-promoted 6-endo-dig thioannulation of o-alkynyl oxime ethers using the cheap and readily available Na2S as the sulfur source. Mechanistic studies disclosed that the reaction proceeded through two C-S bond formations, N-O bond cleavage and the final hydrolysis of imines. This journal is

A new and concise synthesis of 3-aryl- and 3-alkyl-1H-2-benzothiopyran-1-ones (Thioisocoumarins)

Couture,Cornet,Grandclaudon

, p. 1133 - 1134 (2007/10/02)

3-Aryl-and 3-alkyl-1H-2-benzothiopyran-1-ones are readily accessible by reaction of the lithiated N,N-diethyl-o-toluamide (N,N-diethyl-2-methylbenzenecarboxamide) with appropriate aromatic, heteroaromatic and aliphatic thioesters.

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