Production Method 1

1759-58-6

7642-10-6

2532-58-3

28823-41-8

1113-56-0

287-92-3

816-79-5

108-87-2

17618-77-8

7459-71-4

14686-13-6

14686-14-7

2146-38-5

3524-73-0

6443-92-1

Reaction Conditions

1.1 Reagents: Hydrogen Catalysts: Ruthenium phosphide (RuP2) ,  Molybdenum phosphide (MoP) ,  Silica Gel 60 ;  2 h, 600 °C; 600 °C → 450 °C; 15 min, 450 °C
1.2 Reagents: Hydrogen ;  9 h, 100 mbar, 450 °C

Reference

A Highly Stable Bimetallic Transition Metal Phosphide Catalyst for Selective Dehydrogenation of n-Heptane

Stober, Robert; et al, ChemCatChem, 2022, 14(18),

trans-1,3-Dimethylcyclopentane (~70%) Preparation Products

• (3Z)-3-Heptene (7642-10-6)
• Cyclopentane,1,3-dimethyl-, (1R,3S)-rel- (2532-58-3)
• 2,4-Hexadiene,2-methyl- (28823-41-8)
• 2,3-dimethyl-1,3-pentadiene (1113-56-0)
• Cyclopentane (287-92-3)
• 2-Pentene, 3-ethyl- (816-79-5)
• Methylcyclohexane (108-87-2)
• trans-1,3-Dimethylcyclopentane (~70%) (1759-58-6)
• 2-Hexene, 3-methyl- (17618-77-8)
• 3,5-dimethylcyclopentene (7459-71-4)
• 2-Heptene, (2E)- (14686-13-6)
• trans-3-Heptene (14686-14-7)
• 1-Ethyl-1-cyclopentene (2146-38-5)
• 5-Methyl-1-hexene (3524-73-0)
• (Z)-2-Heptene (6443-92-1)

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• Solvents and Organic Chemicals Organic Compounds Hydrocarbons Saturated hydrocarbons Cycloalkanes

• 2532-58-3(Cyclopentane,1,3-dimethyl-, (1R,3S)-rel-)
• 1636-39-1(1,\u200b1'-\u200bBicyclopentyl)
• 1192-18-3((1R,2S)-1,2-dimethylcyclopentane)
• 2098070-20-1(2-(3-(Pyridin-3-yl)-1H-pyrazol-1-yl)acetimidamide)
• 2680771-01-9(4-cyclopentyl-3-{(prop-2-en-1-yloxy)carbonylamino}butanoic acid)
• 1444113-98-7(N-(3-cyanothiolan-3-yl)-2-[(2,2,2-trifluoroethyl)sulfanyl]pyridine-4-carboxamide)
• 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)
• 941977-17-9(N'-(3-chloro-2-methylphenyl)-N-2-(dimethylamino)-2-(naphthalen-1-yl)ethylethanediamide)
• 2138166-62-6(2,2-Difluoro-3-[methyl(2-methylbutyl)amino]propanoic acid)