Production Method 1

111-70-6

690-08-4

141-93-5

931-88-4

575-37-1

2146-37-4

930-18-7

19037-72-0

624-64-6

52161-57-6

16327-38-1

824-90-8

622-96-8

264-09-5

3404-65-7

616-12-6

691-38-3

824-22-6

14686-13-6

2808-79-9

Reaction Conditions

1.1 Catalysts: Vanadium ;  100 - 550 °C

Reference

Catalytic conversion of alcohols having at least three carbon atoms to hydrocarbon blendstock

, World Intellectual Property Organization, , ,

2-Pentene,4,4-dimethyl-, (2E)- Raw materials

• 1-Heptanol

2-Pentene,4,4-dimethyl-, (2E)- Preparation Products

• 1,3-DIETHYLBENZENE (141-93-5)
• Cyclooctene (931-88-4)
• 1,7-Dimethylnaphthalene (575-37-1)
• Ethylidenecyclopentane (2146-37-4)
• Cyclopropane,1,2-dimethyl-, (1R,2S)-rel- (930-18-7)
• 2-Pentene,4,4-dimethyl-, (2E)- (690-08-4)
• Cyclopentene,4,4-dimethyl- (19037-72-0)
• 2-BUTENE (624-64-6)
• Benzene, 1-methyl-3-(1-methyl-2-propenyl)- (52161-57-6)
• Cyclobutene, 3,3-dimethyl- (16327-38-1)
• Benzene, 1-buten-1-yl- (824-90-8)
• 4-Ethyltoluene (622-96-8)
• 7H-Benzocycloheptene (264-09-5)
• 3-methyl-3-hexene (c,t) (3404-65-7)
• 2-Pentene, 3-methyl-,(2E)- (616-12-6)
• cis-4-Methyl-2-pentene (691-38-3)
• 4-Methylindan (824-22-6)
• 2-Heptene, (2E)- (14686-13-6)
• Cyclohexene,1,4-dimethyl- (2808-79-9)

• 1. Evolution and characterization of a benzylguanine-binding RNA aptamer?
  J. Xu,T. J. Carrocci,A. A. Hoskins Chem. Commun., 2016,52, 549-552
• 2. Evolution of hierarchical porous structures in supramolecular guest–host hydrogels?
  Christopher B. Rodell,Christopher B. Highley,Minna H. Chen,Neville N. Dusaj,Chao Wang,Lin Han,Jason A. Burdick Soft Matter, 2016,12, 7839-7847
• 3. Establishing new scaling relations on two-dimensional MXenes for CO2 electroreduction?
  Albertus D. Handoko,Khoong Hong Khoo,Teck Leong Tan,Hongmei Jin,Zhi Wei Seh J. Mater. Chem. A, 2018,6, 21885-21890
• 4. Fate of nitrogen-15 in the subsequent growing season of greenhouse tomato plants (Lycopersicon esculentum Mill) as influenced by alternate partial root-zone irrigation
  Maomao Hou,Fenglin Zhong,Qiu Jin,Enjiang Liu,Jie Feng,Tengyun Wang,Yue Gao RSC Adv., 2017,7, 34392-34400
• 5. Evolutionary de novo design of phenothiazine derivatives for dye-sensitized solar cells?
  Vishwesh Venkatraman,Marco Foscato,Vidar R. Jensen,Bj?rn K?re Alsberg J. Mater. Chem. A, 2015,3, 9851-9860

• Solvents and Organic Chemicals Organic Compounds Hydrocarbons Unsaturated hydrocarbons Unsaturated aliphatic hydrocarbons

• 19550-75-5(trans-2,2-Dimethyl-3-heptene)
• 3123-93-1(3-Hexene, 2,2-dimethyl-)
• 692-70-6(CIS-2,5-DIMETHYL-3-HEXENE)
• 691-38-3(cis-4-Methyl-2-pentene)
• 690-92-6(cis-2,2-Dimethyl-3-hexene)
• 674-76-0(2-Pentene, 4-methyl-,(2E)-)
• 10557-44-5(3-Hexene, 2,5-dimethyl-, (Z)-)
• 332062-08-5(Fmoc-S-3-amino-4,4-diphenyl-butyric acid)
• 1270529-38-8(1,2,3,4,5,6-Hexahydro-[2,3]bipyridinyl-6-ol)
• 2680771-01-9(4-cyclopentyl-3-{(prop-2-en-1-yloxy)carbonylamino}butanoic acid)