Brassinazole - ≥90%(HPLC)(Mixed spin) , CAS No.224047-41-0

CAS: 224047-41-0 Cat. No.: B152405 Formula: C₁₈H₁₈ClN₃O Peso molecolare: 327.81 Numero EC: 678-200-8

QUALITÀ & PUREZZA ≥90%(HPLC)(Mixed spin)

Synonyms

BRZ|2,3-cs/ex-PinD|Sodium tetraborate (Na2B4O7)|4-(4-chlorophenyl)-2-phenyl-3-(1,2,4-triazol-1-yl)-2-butanol|(Rac)-Brassinazole|1H-1,2,4-Triazole-1-ethanol, beta-((4-chlorophenyl)methyl)-alpha-methyl-alpha-phenyl-|S(+)--Vigabatrin|Brassinazole|4-(4-Chloro-phenyl)-2-phenyl-3-[1,2,4]triazol-1-yl-butan-2-ol|1H-1,2,4-TRIAZOLE-1-ETHANOL, .BETA.-((4-CHLOROPHENYL)METHYL)-.ALPHA.-METHYL-.ALPHA.-PHENYL-|3-(4-Chlorophenyl)-1-methyl-1-phenyl-2-(1,2,4-triazol-1-yl)-1-propanol|4-(4-chlorophenyl)-2-phenyl-3-(1H-1,2,4-triazol-1-yl)butan-2-ol|1-[2-(4-Chlorophenyl)-1-(1-hydroxy-1-phenylethyl)ethyl]-1,2,4-triazole

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Panoramica

Brassinazole has been used in phenotype analyses to detect morphological changes in G-protein β subunit agb1 mutants.

Specifiche

Sinonimi

BRZ | 2,3-cs/ex-PinD | Sodium tetraborate (Na2B4O7) | 4-(4-chlorophenyl)-2-phenyl-3-(1,2,4-triazol-1-yl)-2-butanol | (Rac)-Brassinazole | 1H-1,2,4-Triazole-1-ethanol, beta-((4-chlorophenyl)methyl)-alpha-methyl-alpha-phenyl- | S(+)--Vigabatrin | Brassinazole | 4-(4-Chloro-phenyl)-2-phenyl-3-[1,2,4]triazol-1-yl-butan-2-ol | 1H-1,2,4-TRIAZOL Mostra altro

Specifiche e purezza

≥90%(HPLC)(Mixed spin)

Meccanismi biochimici e fisiologici

Brassinazole can induce dwarfing and morphological changes in Arabidopsis thaliana, which results in similarity with brassinol-deficient mutants. These changes were neutralized by brassinolide treatment, suggesting that brassinazole was responsible for br

Condizioni di conservazione di stoccaggio

Store at -20°C

Spedito in

Ice chest + Ice pads

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Purezza

≥90%(HPLC)(Mixed spin)

Nomi e identificatori

Pubchem Sid

488198900

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488198900

Sorrisi canonici

CC(C1=CC=CC=C1)(C(CC2=CC=C(C=C2)Cl)N3C=NC=N3)O

IUPAC Name

4-(4-chlorophenyl)-2-phenyl-3-(1,2,4-triazol-1-yl)butan-2-ol

InChIKey

YULDTPKHZNKFEY-UHFFFAOYSA-N

INCHI

1S/C18H18ClN3O/c1-18(23,15-5-3-2-4-6-15)17(22-13-20-12-21-22)11-14-7-9-16(19)10-8-14/h2-10,12-13,17,23H,11H2,1H3

Isomeri SMILES

CC(C1=CC=CC=C1)(C(CC2=CC=C(C=C2)Cl)N3C=NC=N3)O

Peso molecolare

327.81

Reaxy-Rn

8267246

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=8267246&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Phenylpropanoids and polyketides
    • Classe Linear 1,3-diarylpropanoids

• Kingdom: Organic compounds
• Superclass: Phenylpropanoids and polyketides
• Classe: Linear 1,3-diarylpropanoids
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Linear 1,3-diarylpropanoids
• Alternative Parents: Amphetamines and derivatives Chlorobenzenes Aryl chlorides Triazoles Tertiary alcohols Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organochlorides Hydrocarbon derivatives Aromatic alcohols
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Linear 1,3-diarylpropanoid - Amphetamine or derivatives - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Benzenoid - Azole - Heteroaromatic compound - 1,2,4-triazole - Tertiary alcohol - Azacycle - Organoheterocyclic compound - Organochloride - Organohalogen compound - Aromatic alcohol - Organic nitrogen compound - Alcohol - Hydrocarbon derivative - Organopnictogen compound - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Aromatic heteromonocyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as linear 1,3-diarylpropanoids. These are organic compounds with a structure based on a C6-C3-C6 skeleton, where the two benzene rings are not linked together.
• External Descriptors: tertiary alcohol - monochlorobenzenes - triazoles

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

Obiettivi associati (non umani)

Oryza sativa (2923 Activities)

Explore this target

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

Meccanismi d'azione

Proprietà chimiche e fisiche

• Solubilità: 66 mg/mL(201.34 mM) in DMSO；4 mg/mL (12.20 mM) in Ethanol；Water（Insoluble ）
• Peso molecolare: 327.800 g/mol
• XLogP3: 3.600
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 5
• Exact Mass: 327.114 Da
• Monoisotopic Mass: 327.114 Da
• Topological Polar Surface Area: 50.900 Ų
• Heavy Atom Count: 23
• Formal Charge: 0
• Complexity: 369.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 2
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1