N-(4-hydroxy-6-methyl-5-nitropyrimidin-2-yl)acetamide

95%

Reagent Code: #219072
fingerprint
CAS Number 299916-90-8

science Other reagents with same CAS 299916-90-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 212.16 g/mol
Formula C₇H₈N₄O₄
badge Registry Numbers
MDL Number MFCD31555304
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of sulfonylurea herbicides, particularly in the production of agrochemicals that target broadleaf weeds and grasses in crops like rice and wheat. Its structure enables the formation of active herbicidal compounds that inhibit plant acetolactate synthase (ALS), disrupting amino acid synthesis in susceptible weeds. Due to its nitro and hydroxyl functional groups, it participates in selective coupling reactions, making it valuable in developing environmentally low-impact herbicides with high potency at low application rates.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿24,910.00
inventory 250mg
10-20 days ฿45,990.00
inventory 1g
10-20 days ฿91,990.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
N-(4-hydroxy-6-methyl-5-nitropyrimidin-2-yl)acetamide
No image available

Used as a key intermediate in the synthesis of sulfonylurea herbicides, particularly in the production of agrochemicals that target broadleaf weeds and grasses in crops like rice and wheat. Its structure enables the formation of active herbicidal compounds that inhibit plant acetolactate synthase (ALS), disrupting amino acid synthesis in susceptible weeds. Due to its nitro and hydroxyl functional groups, it participates in selective coupling reactions, making it valuable in developing environmentally low

Used as a key intermediate in the synthesis of sulfonylurea herbicides, particularly in the production of agrochemicals that target broadleaf weeds and grasses in crops like rice and wheat. Its structure enables the formation of active herbicidal compounds that inhibit plant acetolactate synthase (ALS), disrupting amino acid synthesis in susceptible weeds. Due to its nitro and hydroxyl functional groups, it participates in selective coupling reactions, making it valuable in developing environmentally low-impact herbicides with high potency at low application rates.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...