(+)-Pulegone - 10mM in DMSO , CAS No.89-82-7

CAS: 89-82-7 Cat. No.: P426743 Summenformel: C₁₀H₁₆O Molekulargewicht: 152.24 EG-Nummer: 201-943-2 PubChem CID: 442495

GRADE & PURITY 10mM in DMSO

Synonyms

(5R)-5-methyl-2-(propan-2-ylidene)cyclohexanone | (R)-5-methyl-2-(propan-2-ylidene)cyclohexanone | C09893 | DTXCID6030312 | Pulegone,(S) | SCHEMBL38305 | doi:10.14272/NZGWDASTMWDZIW-MRVPVSSYSA-N.1 | R-(+)-Pulegone | STK801810 | DTXCID405975 | Tox21_200206

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Übersicht

(R)-(+)-Pulegone, a monoterpene ketone found in essential oil of pennyroyal,[1] can induce abortion.
(R)-(+)-Pulegone may be used as a starting material to synthesize: · (2S,4R,6R,8S)-2,4,8-trimethyl-1,7-dioxaspiro[5.5]undecane, a spiroketal · (R)-(+)-citronellic acid, an intermediate to prepare leucine-d3 · (+)-fawcettidine, a Lycopodium alkaloid

Specifications

Synonyme

(5R)-5-methyl-2-(propan-2-ylidene)cyclohexanone | (R)-5-methyl-2-(propan-2-ylidene)cyclohexanone | C09893 | DTXCID6030312 | Pulegone,(S) | SCHEMBL38305 | doi:10.14272/NZGWDASTMWDZIW-MRVPVSSYSA-N.1 | R-(+)-Pulegone | STK801810 | DTXCID405975 | Tox21_200206

Spezifikationen & Reinheit

10mM in DMSO

Storage

Store at -80°C

Verschickt in

Dry ice packs + Cold packs

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Aktionsart

ACTIVATOR

Namen und Kennungen

• Pubchem Sid: 528752702
• Kanonisches Lächeln: CC1CCC(=C(C)C)C(=O)C1
• IUPAC Name: (5R)-5-methyl-2-propan-2-ylidenecyclohexan-1-one
• InChIKey: NZGWDASTMWDZIW-MRVPVSSYSA-N
• INCHI: 1S/C10H16O/c1-7(2)9-5-4-8(3)6-10(9)11/h8H,4-6H2,1-3H3/t8-/m1/s1
• Isomere SMILES: C[C@@H]1CCC(=C(C)C)C(=O)C1
• WGK Deutschland: 3
• RTECS: OT0261000
• PubChem CID: 442495
• Molekulargewicht: 152.24

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Klasse Prenol lipids
      • Subclass Monoterpenoids

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Klasse: Prenol lipids
• Subclass: Monoterpenoids
• Intermediate Tree Nodes: Not available
• Direct Parent: Menthane monoterpenoids
• Alternative Parents: Monocyclic monoterpenoids Cyclic ketones Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aliphatic homomonocyclic compounds
• Substituents: P-menthane monoterpenoid - Monocyclic monoterpenoid - Cyclic ketone - Ketone - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic homomonocyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as menthane monoterpenoids. These are monoterpenoids with a structure based on the o-, m-, or p-menthane backbone. P-menthane consists of the cyclohexane ring with a methyl group and a (2-methyl)-propyl group at the 1 and 4 ring position, respectively. The o- and m- menthanes are much rarer, and presumably arise by alkyl migration of p-menthanes.
• External Descriptors: Menthane monoterpenoids

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

Zugehörige Ziele (nicht menschlich)

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Zea mays (820 Activities)

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Meloidogyne incognita (862 Activities)

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Musca domestica (713 Activities)

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Columba livia (47 Activities)

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Rattus norvegicus (775804 Activities)

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Rdl GABA receptor subunit (76 Activities)

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Meloidogyne javanica (98 Activities)

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Frankliniella occidentalis (90 Activities)

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Wirkungsmechanismen

Chemische und physikalische Eigenschaften

• Brechungsindex: 1.49
• Spezifische Drehung [α]: 23° (neat)
• Flammpunkt (°F): 179.6 °F
• Flammpunkt (°C): 82°C
• Siedepunkt (°C): 224 °C
• Molekulargewicht: 152.230 g/mol
• XLogP3: 2.800
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 152.12 Da
• Monoisotopic Mass: 152.12 Da
• Topological Polar Surface Area: 17.100 Ų
• Heavy Atom Count: 11
• Formal Charge: 0
• Complexity: 197.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 1
• 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

Referenzen

1. Huimin Liao, Jinghong Wang, Feiran Chen, Le Ya, Ningke Fan, Yinghua Shu, Zhenggao Xiao, Zhenyu Wang.  (2024)  Salicylic acid functionalized chitosan nanocomposite increases bioactive components and insect resistance of Agastache rugosa.  PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY,      [PMID:39477584] [10.1016/j.pestbp.2024.106131]