Name: Nicosulfuron - analytical standard , CAS No.111991-09-4
Brand: Aladdin Scientific
SKU: N110042
Availability: InStock

Nicosulfuron - analytical standard , CAS No.111991-09-4

CAS: 111991-09-4 Cat. No.: N110042 Formule: C₁₅H₁₈N₆O₆S Poids moléculaire: 410.41 Numéro CE: 601-148-4

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Nicosulfuron - analytical standard CAS No(111991-09-4) by Aladdin Scientific

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DISPONIBLE À COMMANDE

QUALITÉ & PURETÉ Analytical standard ?

Synonyms

1-(4,6-Dimethoxy-2-pyrimidinyl)-3-[3-(dimethylcarbamoyl)-2-pyridylsulfonyl]urea|2-[N-[(4,6-Dimethoxypyrimidin-2-yl)carbamoyl]sulfamoyl]-N,N-dimethylnicotinamide

Storage

Store at -20°C,Argon charged

Shipped In

Ice chest + Ice pads

Fiche de spécifications

Spécifications Noms et identifiants Données avancées Taxonomic Classification Structure 3D Cibles associées (non humaines) Mécanismes d'action Certificats (CoA, COO, BSE/TSE et tableau d'analyse) Propriétés chimiques et physiques Citations of This Product Calculateurs de solution Avis

Spécifications

Synonymes

1-(4,6-Dimethoxy-2-pyrimidinyl)-3-[3-(dimethylcarbamoyl)-2-pyridylsulfonyl]urea | 2-[N-[(4,6-Dimethoxypyrimidin-2-yl)carbamoyl]sulfamoyl]-N,N-dimethylnicotinamide

Spécifications et pureté

analytical standard

Conditions de stockage de stockage

Store at -20°C,Argon charged

Expédié en

Ice chest + Ice pads

Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.

Grade

Analytical standard

Noms et identifiants

Pubchem Sid

528773116

Sourires canoniques

CN(C)C(=O)C1=C(N=CC=C1)S(=O)(=O)NC(=O)NC2=NC(=CC(=N2)OC)OC

IUPAC Name

2-[(4,6-dimethoxypyrimidin-2-yl)carbamoylsulfamoyl]-N,N-dimethylpyridine-3-carboxamide

InChIKey

RTCOGUMHFFWOJV-UHFFFAOYSA-N

INCHI

1S/C15H18N6O6S/c1-21(2)13(22)9-6-5-7-16-12(9)28(24,25)20-15(23)19-14-17-10(26-3)8-11(18-14)27-4/h5-8H,1-4H3,(H2,17,18,19,20,23)

Isomères SMILES

CN(C)C(=O)C1=C(N=CC=C1)S(=O)(=O)NC(=O)NC2=NC(=CC(=N2)OC)OC

WGK Allemagne

RTECS

US4615000

Numéro ONU

3077

Groupe d'emballage

III

Poids moléculaire

410.41

Reaxy-Rn

7233432

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=7233432&ln=

Données avancées

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organoheterocyclic compounds
  - Classe Pyridines and derivatives
    - Subclass Pyridinesulfonamides

Kingdom	Organic compounds
Superclass	Organoheterocyclic compounds
Classe	Pyridines and derivatives
Subclass	Pyridinesulfonamides
Intermediate Tree Nodes	Not available
Direct Parent	Pyridinesulfonamides
Alternative Parents	Nicotinamides Sulfonylureas Alkyl aryl ethers Pyrimidines and pyrimidine derivatives Tertiary carboxylic acid amides Organosulfonic acids and derivatives Heteroaromatic compounds Aminosulfonyl compounds Propargyl-type 1,3-dipolar organic compounds Carboximidic acids and derivatives Azacyclic compounds Organopnictogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework	Aromatic heteromonocyclic compounds
Substituents	Pyridine-2-sulfonamide - Nicotinamide - Pyridinecarboxamide - Pyridine carboxylic acid or derivatives - Alkyl aryl ether - Sulfonylurea - Pyrimidine - Heteroaromatic compound - Organic sulfonic acid or derivatives - Aminosulfonyl compound - Tertiary carboxylic acid amide - Sulfonyl - Organosulfonic acid or derivatives - Carboxamide group - Carboximidic acid derivative - Carboxylic acid derivative - Ether - Azacycle - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organooxygen compound - Organonitrogen compound - Organopnictogen compound - Organosulfur compound - Organic oxide - Hydrocarbon derivative - Organic oxygen compound - Organic nitrogen compound - Aromatic heteromonocyclic compound
Description	This compound belongs to the class of organic compounds known as pyridinesulfonamides. These are heterocyclic compounds containing a pyridine ring substituted by one or more sulfonamide groups.
External Descriptors	Sulfonylurea herbicides
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Structure 3D

Cibles associées (non humaines)

Echinochloa crus-galli (3685 Activities)

Lot Number	Certificate Type	Date	Article
H2408639	Certificate of Analysis	May 19, 2026	N110042
H2307116	Certificate of Analysis	Aug 14, 2023	N110042
G2209178	Certificate of Analysis	Jul 15, 2022	N110042

Solubilité	400mg/kg water (pH buffered, final pH 5.01), 120g/kg (pH7 buffered, final pH 6.85), 39.2g/kg (pH9 buffered, final pH 8.8), solubility in organic solvents (g/kg): acetone 18, acetonitrile 23, chloroform and dimethylformamide 64, dichloromethane 160, ethano
Sensibilité	Air sensitive
Point de fusion (°C)	142°C
Poids moléculaire	410.400 g/mol
XLogP3	0.600
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	9
Rotatable Bond Count	6
Exact Mass	410.101 Da
Monoisotopic Mass	410.101 Da
Topological Polar Surface Area	161.000 Å²
Heavy Atom Count	28
Formal Charge	0
Complexity	642.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

Nicosulfuron - analytical standard , CAS No.111991-09-4

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