Picloram - ≥95% , CAS No.1918-02-1

CAS: 1918-02-1 Cat. No.: P141070 Formule: C₆H₃Cl₃N₂O₂ Poids moléculaire: 241.46 Beilstein Registry Number: 479075 Numéro CE: 217-636-1

QUALITÉ & PURETÉ ≥95%

Synonyms

WOM | 4-Amino-3,6-trichloro-2-picolinic acid | 4-Amino-3,6-trichlorpicolinsaeure | STK179674 | Picloram [ANSI:BSI:ISO] | PICLORAM [MI] | 2-Pyridinecarboxylic acid, 4-amino-3,5,6-trichloro- | 3,6-Trichloro-4-aminopicolinic acid | Tordon 22K | 4-Amino-3,5,6

Storage

Argon charged,Room temperature

Shipped In

Normal

Vue d’ensemble

Atrazine has been used as a supplement in the growth medium of embryos. 

Spécifications

Synonymes

WOM | 4-Amino-3,6-trichloro-2-picolinic acid | 4-Amino-3,6-trichlorpicolinsaeure | STK179674 | Picloram [ANSI:BSI:ISO] | PICLORAM [MI] | 2-Pyridinecarboxylic acid, 4-amino-3,5,6-trichloro- | 3,6-Trichloro-4-aminopicolinic acid | Tordon 22K | 4-Amino-3,5,6

Spécifications et pureté

≥95%

Mécanismes biochimiques et physiologiques

4-amino-3,5,6-trichloropyridine-2-carboxylic acid (4-amino-3,5,6-trichloropyridine-2-carboxylic acid) is a chlorinated herbicide widely used in the control of woody plants and broad-leaved weeds. Atrazine can induce direct somatic embryogenesis of Lilium

Conditions de stockage de stockage

Argon charged,Room temperature

Expédié en

Normal

Pureté

≥95%

Noms et identifiants

Pubchem Sid

508813861

Sourires canoniques

C1(=C(C(=NC(=C1Cl)Cl)C(=O)O)Cl)N

IUPAC Name

4-amino-3,5,6-trichloropyridine-2-carboxylic acid

InChIKey

NQQVFXUMIDALNH-UHFFFAOYSA-N

INCHI

1S/C6H3Cl3N2O2/c7-1-3(10)2(8)5(9)11-4(1)6(12)13/h(H2,10,11)(H,12,13)

Isomères SMILES

C1(=C(C(=NC(=C1Cl)Cl)C(=O)O)Cl)N

WGK Allemagne

2

RTECS

TJ7525000

Poids moléculaire

241.46

Beilstein

479075

Reaxy-Rn

479075

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=479075&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Classe Pyridines and derivatives
      • Subclass Pyridinecarboxylic acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Classe: Pyridines and derivatives
• Subclass: Pyridinecarboxylic acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Pyridinecarboxylic acids
• Alternative Parents: Polyhalopyridines 2-halopyridines Aminopyridines and derivatives Aryl chlorides Vinylogous halides Heteroaromatic compounds Amino acids Azacyclic compounds Carboxylic acids Monocarboxylic acids and derivatives Organopnictogen compounds Primary amines Organochlorides Organic oxides Hydrocarbon derivatives Organooxygen compounds
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Pyridine carboxylic acid - Polyhalopyridine - Aminopyridine - 2-halopyridine - Aryl chloride - Aryl halide - Heteroaromatic compound - Vinylogous halide - Amino acid or derivatives - Amino acid - Carboxylic acid derivative - Azacycle - Carboxylic acid - Monocarboxylic acid or derivatives - Amine - Organonitrogen compound - Organochloride - Organohalogen compound - Organooxygen compound - Primary amine - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Aromatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as pyridinecarboxylic acids. These are compounds containing a pyridine ring bearing a carboxylic acid group.
• External Descriptors: Pyridine herbicides

Data sources

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

Cibles associées (humaines)

ESR1 Tclin Estrogen receptor alpha (17718 Activities)

Discover Target: ESR1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

AR Tclin Androgen Receptor (11781 Activities)

Discover Target: AR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

MAOA Tclin Monoamine oxidase A (11911 Activities)

Discover Target: MAOA

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

THRB Tclin Thyroid hormone receptor beta-1 (7926 Activities)

Discover Target: THRB

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

RXRA Tclin Retinoid X receptor alpha (3637 Activities)

Discover Target: RXRA

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)

Discover Target: TDP1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Cibles associées (non humaines)

Ppard Peroxisome proliferator-activated receptor delta (358 Activities)

Discover Target: Ppard

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Mécanismes d'action

Propriétés chimiques et physiques

• Solubilité: Soluble in acetone
• Sensibilité: Moisture sensitive
• Point de fusion (°C): 200°C
• Poids moléculaire: 241.500 g/mol
• XLogP3: 2.200
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 1
• Exact Mass: 239.926 Da
• Monoisotopic Mass: 239.926 Da
• Topological Polar Surface Area: 76.200 Ų
• Heavy Atom Count: 13
• Formal Charge: 0
• Complexity: 216.000
• 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