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N-(4-chlorophenyl)-5,6-dihydro-4H-1,3-thiazin-2-amine is an organic compound with a chemical structure that features a thiazin ring fused with a dihydro ring and a chlorophenyl group. It is known for its reactivity and utility in the synthesis of various pharmaceutical compounds.

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  • 103039-04-9 Structure
  • Basic information

    1. Product Name: N-(4-chlorophenyl)-5,6-dihydro-4H-1,3-thiazin-2-amine
    2. Synonyms: N-(4-chlorophenyl)-5,6-dihydro-4H-1,3-thiazin-2-amine
    3. CAS NO:103039-04-9
    4. Molecular Formula: C10H11ClN2S
    5. Molecular Weight: 226.72574
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 103039-04-9.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: N-(4-chlorophenyl)-5,6-dihydro-4H-1,3-thiazin-2-amine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(4-chlorophenyl)-5,6-dihydro-4H-1,3-thiazin-2-amine(103039-04-9)
    11. EPA Substance Registry System: N-(4-chlorophenyl)-5,6-dihydro-4H-1,3-thiazin-2-amine(103039-04-9)
  • 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: 103039-04-9(Hazardous Substances Data)

103039-04-9 Usage

Uses

Used in Pharmaceutical Synthesis:
N-(4-chlorophenyl)-5,6-dihydro-4H-1,3-thiazin-2-amine is used as a synthetic reagent for the production of various pharmaceutical compounds. Its unique structure allows it to be a key component in the creation of analogs of levamisole, a drug used to treat certain types of parasitic infections.
Additionally, this compound is utilized in the synthesis of thiazoline derivatives, which are known for their diverse biological activities, including antimicrobial, antifungal, and anti-inflammatory properties.
Furthermore, N-(4-chlorophenyl)-5,6-dihydro-4H-1,3-thiazin-2-amine is also used in the development of analogs of intravenous anesthetics. These analogs can potentially offer improved efficacy, safety, and reduced side effects compared to existing anesthetic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 103039-04-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,0,3 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 103039-04:
(8*1)+(7*0)+(6*3)+(5*0)+(4*3)+(3*9)+(2*0)+(1*4)=69
69 % 10 = 9
So 103039-04-9 is a valid CAS Registry Number.

103039-04-9Downstream Products

103039-04-9Relevant articles and documents

Aminothiazines et aminothiazoles analogues ouverts du levamisole: synthese et approche du mode d'action nematicide

Caujolle, Raymond,Amarouch, Hamid,Payard, Marc,Loiseau, Philippe R.,Bories, Christian,et al.

, p. 287 - 292 (2007/10/02)

New compounds with thiazoline or dihydrothiazine rings substituted by alkylamino or arylamino groups were synthesized and screened in vitro against three Nematodes.Inhibition of fumarate-reductase activity was also evaluated.For all in vitro anti-parasitic tests, dihydrothiazines were more potent than corresponding thiazolines derivatives, however, thiazolines showed a greater inhibition of fumarate-reductase.

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