4-Methyl-1-cyclohexene - ≥97% , CAS No.591-47-9

CAS: 591-47-9 Cat. No.: M304079 Summenformel: C₆H₉CH₃ Molekulargewicht: 96.17 EG-Nummer: 209-715-4

GRADE & PURITY ≥97%

Synonyms

EN300-103785 | Cyclohexene, 4-methyl- | MFCD00001573 | NSC 9386 | M0201 | 4-METHYLCYCLOHEXENE | 4-methyl-cyclohexene | FT-0618984 | AKOS015842661 | 4-Methyl-1-cyclohexene | 4-Methylcyclohexene-1 | 4-Methylcyclohexene, 99% | 2N22W8H0JX | DTXSID10862257 | U

Storage

Room temperature,Desiccated

Shipped In

FedEx DG Service

Übersicht

Application：

4-Methyl-1-cyclohexene is used in the synthesis of an enantiomerically pure oxaliplatin derivative, {(1R,2R,4R)-4-Methyl-1,2-cyclohexanediamine}oxalatoplatinum(II), which exhibits good anticancer activity. It is also used in the preparation of N,N-diethyldithiocarbamate functionalized 1,4-polyisoprenes.

Specifications

Synonyme

EN300-103785 | Cyclohexene, 4-methyl- | MFCD00001573 | NSC 9386 | M0201 | 4-METHYLCYCLOHEXENE | 4-methyl-cyclohexene | FT-0618984 | AKOS015842661 | 4-Methyl-1-cyclohexene | 4-Methylcyclohexene-1 | 4-Methylcyclohexene, 99% | 2N22W8H0JX | DTXSID10862257 | U

Spezifikationen & Reinheit

≥97%

Storage

Room temperature,Desiccated

Verschickt in

FedEx DG Service

Reinheit

≥97%

Namen und Kennungen

• Pubchem Sid: 508809641
• Kanonisches Lächeln: CC1CCC=CC1
• IUPAC Name: 4-methylcyclohexene
• InChIKey: FSWCCQWDVGZMRD-UHFFFAOYSA-N
• INCHI: 1S/C7H12/c1-7-5-3-2-4-6-7/h2-3,7H,4-6H2,1H3
• Isomere SMILES: CC1CCC=CC1
• WGK Deutschland: 3
• Molekulargewicht: 96.17
• Reaxy-Rn: 1901299
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1901299&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Hydrocarbons
    • Klasse Unsaturated hydrocarbons
      • Subclass Olefins
        • Ebene5 Cyclic olefins
          • Ebene6 Cycloalkenes

• Kingdom: Organic compounds
• Superclass: Hydrocarbons
• Klasse: Unsaturated hydrocarbons
• Subclass: Olefins
• Intermediate Tree Nodes: Cyclic olefins
• Direct Parent: Cycloalkenes
• Alternative Parents: Unsaturated aliphatic hydrocarbons
• Molecular Framework: Aliphatic homomonocyclic compounds
• Substituents: Cycloalkene - Unsaturated aliphatic hydrocarbon - Aliphatic homomonocyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as cycloalkenes. These are unsaturated monocyclic hydrocarbons having one endocyclic double bond.
• External Descriptors: Not available

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

Chemische und physikalische Eigenschaften

• Brechungsindex: 1.4400-1.4420
• Flammpunkt (°F): 19.4 °F
• Flammpunkt (°C): -7 °C
• Siedepunkt (°C): 104°C
• Molekulargewicht: 96.170 g/mol
• XLogP3: 2.700
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 0
• Exact Mass: 96.0939 Da
• Monoisotopic Mass: 96.0939 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 7
• Formal Charge: 0
• Complexity: 72.100
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 1
• 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. Shihao Su, Guojun Lv, Xuyang Zou, Jiangzhang Wang, Chaoyi Zhou, Yan Chen, Jialing Shen, Yangbin Shen, Zhongmin Liu.  (2023)  Room-temperature tandem conversion of cyclic alkenes into 1,2-diols using molecular oxygen and β-MnO2 heterogeneous catalyst.  GREEN CHEMISTRY,      [PMID:] [10.1039/D3GC02863A]

2. Yan Chen, Guojun Lv, Xuyang Zou, Shihao Su, Jiangzhang Wang, Chaoyi Zhou, Jialing Shen, Yangbin Shen, Zhongmin Liu.  (2024)  High-electrophilic (SiO)2Nb(OH)(=O) sites confined in silanol defects over Nb-Beta zeolite for efficient cyclic alkene epoxidation reactions.  JOURNAL OF COLLOID AND INTERFACE SCIENCE,      [PMID:38490038] [10.1016/j.jcis.2024.03.076]

3. Shihao Su, Guojun Lv, Jialing Shen, Fuxin Wang, Lachgar Oussama, Yan Chen, Shengnan Xu.  (2025)  Pickering Interfacial Tandem Catalysis of Alkenes to 1,2-Diols over Manganese Oxide Catalysts at Room Temperature.  ACS Catalysis,      [PMID:] [10.1021/acscatal.4c06225]

4. Shihao Su, Xuyang Zou, Guojun Lv, Fuxin Wang, Yangbin Shen.  (2025)  One-pot tandem conversion of alkenes into 1,2-diols over efficient bifunctional tin-tungsten oxide catalysts.  JOURNAL OF COLLOID AND INTERFACE SCIENCE,      [PMID:40378450] [10.1016/j.jcis.2025.137875]