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1566-37-6

3-(Methylthio)-6-phenyl-1,2,4-triazin-5-ol, commonly known as Metribuzin, is a systemic herbicide that belongs to the triazine chemical class. It is characterized by its ability to inhibit photosynthesis in plants, leading to their death. Metribuzin is absorbed and translocated within the plant, making it effective at controlling both emerged and germinating weeds. It is applied as a liquid formulation and is considered to have a low environmental impact due to its relatively low toxicity and mobility in the soil.
Used in Agriculture:
3-(Methylthio)-6-phenyl-1,2,4-triazin-5-ol is used as a herbicide for controlling a wide variety of weeds in different crops such as maize, soybeans, wheat, and potatoes. It is effective in managing both emerged and germinating weeds due to its systemic nature, which allows it to be absorbed and translocated within the plant.
Used in Environmental Management:
3-(Methylthio)-6-phenyl-1,2,4-triazin-5-ol is used as a low-impact herbicide for managing weeds in agricultural settings. Its relatively low toxicity and mobility in the soil contribute to its low environmental impact, making it a preferred choice for sustainable weed control practices. However, it is crucial to follow label instructions and safety precautions to minimize any potential risks to the environment and human health.

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  • 1566-37-6 Structure

  • Basic information

    1. Product Name: 3-(METHYLTHIO)-6-PHENYL-1,2,4-TRIAZIN-5-OL
    2. Synonyms: 3-(METHYLTHIO)-6-PHENYL-1,2,4-TRIAZIN-5-OL;3-METHYLSULFANYL-6-PHENYL-[1,2,4]TRIAZIN-5-OL;3-(methylthio)-6-phenyl-1,2,4-triazin-5(2H)-one
    3. CAS NO:1566-37-6
    4. Molecular Formula: C10H9N3OS
    5. Molecular Weight: 219.26
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1566-37-6.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-(METHYLTHIO)-6-PHENYL-1,2,4-TRIAZIN-5-OL(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(METHYLTHIO)-6-PHENYL-1,2,4-TRIAZIN-5-OL(1566-37-6)
    11. EPA Substance Registry System: 3-(METHYLTHIO)-6-PHENYL-1,2,4-TRIAZIN-5-OL(1566-37-6)

  • 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: 1566-37-6(Hazardous Substances Data)

1566-37-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1566-37-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,6 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1566-37:
(6*1)+(5*5)+(4*6)+(3*6)+(2*3)+(1*7)=86
86 % 10 = 6
So 1566-37-6 is a valid CAS Registry Number.

1566-37-6Relevant articles and documents

TRIAZINE DERIVATIVES, THEIR PREPARATION AND THERAPEUTIC APPLICATION THEREOF

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Page/Page column 5-6, (2008/06/13)

The invention relates to triazine derivatives of general formula (I): Wherein R1, R2 and R3 are as defined herein. The invention also relates to a method for preparing these triazine derivatives and to the therapeutic application thereof.

NEW SUBSTITUTED AZATHYMIDINE DERIVATIVES AND THEIR USE IN THE TREATMENT OF BACTERIAL INFECTIOUS DISEASES

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Page/Page column 43; 48, (2008/06/13)

The invention relates to substituted azathymidines and related compounds of formula (I), wherein X is N or CH, and R1, R2 and R3 are as described in the specification, processes for the preparation thereof, pharmaceutical compositions containing the same, the use thereof optionally in combination with one or more other pharmaceutically active compounds as antibacterial agents for the therapy of infective diseases, and a method for the treatment of such diseases. The compounds of formula (I) are reducing selectively the pathogenicity of bacteria within the host, but without affecting the bacteria outside the host environment.

INFLUENCE OF MEDIUM AND TYPE OF SUBSTITUENT ON THE YIELD OF PRODUCTS OF METHYLATION OF 4-SUBSTITUTED 1,2,4-TRIAZINE-3(2H)-THION-5(4H)-ONES

Mironovich, L. M.,Salistyi, S. M.

, p. 888 - 890 (2007/10/03)

We studied the methylation of 4-R-6-R-1,2,4-triazine -3(2H)-thion-5(4H)-ones (R=H, CH3, H2N, (CH3)2NCO, C6H5NN) by methyl iodide in aqueous and aqueous-methanol solutions of NaOH.

Intramolecular Diels-Alder Reactions of 1,2,4-Triazines. Synthesis of Condensed Pyrimidines

Taylor, Edward C.,Pont, Joseph L.

, p. 4287 - 4292 (2007/10/02)

1,2,4-Triazines with C5 tethered dienophilic side chains are sterically constrained to undergo intramolecular Diels-Alder reactions across the N2/C5 triazine positions; elimination of a nitrile from the intermediate adduct (N1 and C6 of the starting 1,2,4

Synthesis of Bridgeheaded Nitrogen Systems. s-Triazolo-as-triazine, s-Triazolo-as-triazine and s-Triazolo-1,3,4-Thiadiazole Ring Systems

Sasaki, Tadashi,Ito, Eikoh

, p. 1353 - 1356 (2007/10/02)

By the reactions of hydrazino-as-triazines (1a-d and 5) with cyanogen bromide were synthesized s-triazolo-as-triazines (2a-d) and (6).Likewise, similar reactions of amino-s-triazolethiols (7a-e) gave s-triazolo-1,3,4-thiadiazoles (8a-d).Compound 2a was brominated to 2g.

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