4-Chloro-6-methoxy-2-(methylthio)-5-nitropyrimidine

95%

Reagent Code: #160852
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CAS Number 56032-35-0

science Other reagents with same CAS 56032-35-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 235.65 g/mol
Formula C₆H₆ClN₃O₃S
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in the synthesis of agricultural chemicals, particularly herbicides and plant growth regulators. Its structure allows for further functionalization to develop compounds with selective activity in crop protection. It is also utilized in the preparation of certain pharmaceuticals where nitropyrimidine derivatives exhibit biological activity. The presence of reactive groups like the methylthio and nitro moieties enables coupling reactions and substitutions to build more complex molecules in agrochemical research and development.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,710.00
inventory 250mg
10-20 days ฿5,560.00
inventory 1g
10-20 days ฿13,880.00
inventory 5g
10-20 days ฿52,000.00

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4-Chloro-6-methoxy-2-(methylthio)-5-nitropyrimidine
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Used as an intermediate in the synthesis of agricultural chemicals, particularly herbicides and plant growth regulators. Its structure allows for further functionalization to develop compounds with selective activity in crop protection. It is also utilized in the preparation of certain pharmaceuticals where nitropyrimidine derivatives exhibit biological activity. The presence of reactive groups like the methylthio and nitro moieties enables coupling reactions and substitutions to build more complex molec

Used as an intermediate in the synthesis of agricultural chemicals, particularly herbicides and plant growth regulators. Its structure allows for further functionalization to develop compounds with selective activity in crop protection. It is also utilized in the preparation of certain pharmaceuticals where nitropyrimidine derivatives exhibit biological activity. The presence of reactive groups like the methylthio and nitro moieties enables coupling reactions and substitutions to build more complex molecules in agrochemical research and development.

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