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4-Chloro-6-(MethoxyMethyl)-2-MethylpyriMidine, also known as Clomazone, is a pyrimidine derivative with the molecular formula C8H10ClNO. It features a chlorine atom at the 4-position and a methoxymethyl group at the 6-position of the pyrimidine ring. This chemical compound is primarily used as a herbicide in agriculture and horticulture.

3122-81-4

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3122-81-4 Usage

Uses

Used in Agriculture and Horticulture:
4-Chloro-6-(MethoxyMethyl)-2-MethylpyriMidine is used as a pre-emergent herbicide for controlling grasses and broadleaf weeds in various crops. It functions by inhibiting the biosynthesis of carotenoids, which are essential pigments for photosynthesis in plants, ultimately leading to the death of the targeted weeds. This helps preserve crop yield and maintain the quality of agricultural and horticultural products.
The use of Clomazone as a herbicide is favored due to its low acute toxicity to mammals, ensuring the safety of humans and animals in the surrounding environment. Additionally, its relatively low environmental persistence minimizes the potential for long-term ecological impact, making it a preferred choice for sustainable agricultural practices.

Check Digit Verification of cas no

The CAS Registry Mumber 3122-81-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,2 and 2 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3122-81:
(6*3)+(5*1)+(4*2)+(3*2)+(2*8)+(1*1)=54
54 % 10 = 4
So 3122-81-4 is a valid CAS Registry Number.

3122-81-4Relevant academic research and scientific papers

Studies on Pyrimidine Derivatives. XXXII. Reaction of 4-Substituted 2,6-Dimethylpyrimidine 1-Oxides with Phosphoryl Chloride

Sakamoto, Takao,Yoshizawa, Hiroshi,Kaneda, Sohichi,Hama, Yoshiaki,Yamanaka, Hiroshi

, p. 4533 - 4538 (2007/10/02)

The reaction of 2,6-dimethyl-4-phenylpyrimidine 1-oxide with phosphoryl chloride gave 4-chloromethyl-2-methyl-6-phenylpyrimidine exclusively.In contrast, 2,6-dimethyl-4-methoxy-pyrimidine 1-oxide and 2,6-dimethyl-4-dimethylaminopyrimidine 1-oxide reacted with the same reagent to give the corresponding 2-chloromethylpyrimidines predominantly.Keywords - pyrimidine N-oxide; chloromethylpyrimidine; phosphoryl chloride; siteselective reaction; substituent effect

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