1189419-41-7

Nicosulfuron-d<sub>6</sub> Chemical Structure
1189419-41-7

Chemical Structure

Nicosulfuron-d6

  • CAS No.: 1189419-41-7
  • Formula:C15H12D6N6O6S
  • Molecular Weight:416.44

IUPAC Name: 2-(N-((4,6-bis(methoxy-d3)pyrimidin-2-yl)carbamoyl)sulfamoyl)-N,N-dimethylnicotinamide

InChIKey: RTCOGUMHFFWOJV-LIJFRPJRSA-N

SMILES: CN(C)C(C1=C(N=CC=C1)S(NC(NC2=NC(OC([2H])([2H])[2H])=CC(OC([2H])([2H])[2H])=N2)=O)(=O)=O)=O

Biological Activity: Nicosulfuron-d6 is the deuterium labeled Nicosulfuron[1]. Nicosulfuron is a selective herbicide belonging to the sulfonylurea family. Nicosulfuron is commonly used as a post-emergence herbicide to protect maize crops from weeds. Nicosulfuron inhibits acetolactate synthase (ALS) enzyme activity[2].

Cat. No. Product Name Purity Description Pricing
HY-B1876S
Nicosulfuron-d6 98.4% Nicosulfuron-d6 is the deuterium labeled Nicosulfuron. Nicosulfuron is a selective herbicide belonging to the sulfonylurea family. Nicosulfuron is commonly used as a post-emergence herbicide to protect maize crops from weeds. Nicosulfuron inhibits acetolactate synthase (ALS) enzyme activity.
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HY-B1876R
Nicosulfuron (Standard) ≥98% Nicosulfuron (Standard) is the analytical standard of Nicosulfuron. This product is intended for research and analytical applications. Nicosulfuron is a selective herbicide belonging to the sulfonylurea family. Nicosulfuron is commonly used as a post-emergence herbicide to protect maize crops from weeds. Nicosulfuron inhibits acetolactate synthase (ALS) enzyme activity.
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HY-B1876
Nicosulfuron 97.27% Nicosulfuron is efficient, harmless, antifungal and selective herbicide belonging to the sulfonylurea family. Nicosulfuron is also a photosynthetic system inhibitor and inhibits acetolactate synthase (ALS) enzyme activity. Nicosulfuron degradation by Plectosphaerella cucumerina AR1 is glucose concentration dependent in planktonic lifestyle. Nicosulfuron enhances the glycolysis pathway and tricarboxylic acid cycle to improve the adaptability of sweet maize. Nicosulfuron reduces the synthesis of branched-chain amino acids (BCAAs), which is proming for maize cultivation.
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