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1566-37-6

1566-37-6

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1566-37-6 Usage

General Description

3-(Methylthio)-6-phenyl-1,2,4-triazin-5-ol, also known as Metribuzin, is a herbicide belonging to the triazine chemical class. It is commonly used to control a wide variety of weeds in a range of crops, including maize, soybeans, wheat, and potatoes. Metribuzin works by inhibiting photosynthesis in plants, ultimately leading to their death. It is a systemic herbicide, meaning it is absorbed and translocated within the plant, making it effective at controlling both emerged and germinating weeds. Metribuzin 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. However, it is important to follow label instructions and safety precautions when using this chemical.

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.

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

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