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320422-69-3

3-[(4-CHLOROPHENYL)SULFANYL]-1-(2-THIENYL)-1-PROPANONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 320422-69-3 Structure

  • Basic information

    1. Product Name: 3-[(4-CHLOROPHENYL)SULFANYL]-1-(2-THIENYL)-1-PROPANONE
    2. Synonyms: 3-[(4-CHLOROPHENYL)SULFANYL]-1-(2-THIENYL)-1-PROPANONE;SALOR-INT L201030-1EA
    3. CAS NO:320422-69-3
    4. Molecular Formula: C13H11ClOS2
    5. Molecular Weight: 282.81
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 320422-69-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    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)SULFANYL]-1-(2-THIENYL)-1-PROPANONE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-[(4-CHLOROPHENYL)SULFANYL]-1-(2-THIENYL)-1-PROPANONE(320422-69-3)
    11. EPA Substance Registry System: 3-[(4-CHLOROPHENYL)SULFANYL]-1-(2-THIENYL)-1-PROPANONE(320422-69-3)

  • 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: 320422-69-3(Hazardous Substances Data)

320422-69-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 320422-69-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,0,4,2 and 2 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 320422-69:
(8*3)+(7*2)+(6*0)+(5*4)+(4*2)+(3*2)+(2*6)+(1*9)=93
93 % 10 = 3
So 320422-69-3 is a valid CAS Registry Number.

320422-69-3Downstream Products

320422-69-3Relevant articles and documents

Generation of a structurally diverse library through alkylation and ring closure reactions using 3-dimethylamino-1-(thiophen-2-yl)propan-1-one hydrochloride

Roman, Gheorghe

, p. 70 - 80 (2013/06/27)

3-Dimethylamino-1-(thiophen-2-yl)propan-1-one hydrochloride (2), a ketonic Mannich base derived from 2-acetylthiophene, was used as a starting material in different types of alkylation and ring closure reactions with a view to generate a structurally diverse library of compounds. Compound 2 reacts with S-alkylated dithiocarbamic acid salts and aryl mercaptans to produce dithiocarbamates and thioethers, respectively. The dimethylamino moiety in compound 2 was exchanged with various aliphatic secondary and aromatic primary and secondary amines, whereas monocyclic NH-azoles such as pyrazole, imidazole, 1,2,4-triazole, and tetrazole were N-alkylated by compound 2. Ketones, pyrrole and indoles have been the substrates subjected to C-alkylation reactions by compound 2. Ring closure reactions of compound 2 with a suitable bifunctional nucleophile yielded pyrazolines, pyridines, 2,3-dihydro-1,5-1H-benzodiazepines, 2,3-dihydro-1,5-1H- benzothiazepine, pyrimido[1,2-a]benzimidazole and 4-hydroxypiperidine derivatives.

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