6-Chloro-4-ethoxy-2-methylsulfonylpyrimidine

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Reagent Code: #164561
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CAS Number 142596-33-6

science Other reagents with same CAS 142596-33-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 236.676 g/mol
Formula C₇H₉ClN₂O₃S
badge Registry Numbers
MDL Number MFCD18837184
inventory_2 Storage & Handling
Density 1.391 g/cm3
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and plant growth regulators. Its structure allows for further functionalization to develop compounds with selective activity against broadleaf weeds. Also employed in the preparation of certain pharmaceuticals where pyrimidine derivatives are needed for biological activity, including antimicrobials, antivirals, and cancer therapeutics. The chloro and methylsulfonyl groups serve as reactive sites for nucleophilic substitution, making it valuable in multi-step organic synthesis.

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inventory 1g
10-20 days ฿28,680.00

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6-Chloro-4-ethoxy-2-methylsulfonylpyrimidine
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Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and plant growth regulators. Its structure allows for further functionalization to develop compounds with selective activity against broadleaf weeds. Also employed in the preparation of certain pharmaceuticals where pyrimidine derivatives are needed for biological activity, including antimicrobials, antivirals, and cancer therapeutics. The chloro and methylsulfonyl groups serve as reactive sites for nucleophilic substit

Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and plant growth regulators. Its structure allows for further functionalization to develop compounds with selective activity against broadleaf weeds. Also employed in the preparation of certain pharmaceuticals where pyrimidine derivatives are needed for biological activity, including antimicrobials, antivirals, and cancer therapeutics. The chloro and methylsulfonyl groups serve as reactive sites for nucleophilic substitution, making it valuable in multi-step organic synthesis.

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