Production Method 1

496-11-7

496-11-7

Reaction Conditions

1.1 Reagents: Iron ,  Bromine Solvents: Hexane
2.1 Reagents: Butyllithium Solvents: Diethyl ether
2.2 -

Reference

The intermediate formation of [4]metacyclophane on flash vacuum thermolysis

Kostermans, Gerardus B. M.; et al, Journal of Organic Chemistry, 1988, 53(19), 4531-4

Production Method 2

496-11-7

876-02-8

90-00-6

93-51-6

581-42-0

39151-19-4

6443-69-2

90-05-1

767-59-9

Reaction Conditions

1.1 250 h

Reference

Catalytic pyrolysis of lignin over hierarchical HZSM 5 zeolites prepared by post-treatment with alkaline solutions

Tang, Songshan; et al, Journal of Analytical and Applied Pyrolysis, 2019, 137, 86-95

Production Method 3

496-11-7

141-93-5

629-50-5

99-62-7

1074-92-6

17171-71-0

Reaction Conditions

1.1 Catalysts: Zinc ;  6 h, 1 bar, 420 °C

Reference

Renewable p-Xylene Production by Catalytic Conversion of Crude Bioglycerol (GTA-pX Process)

Singh, Vijendra ; Arumugam, Selvamani ; Kumar, Mahesh; Tathod, Anup Prakash; Viswanadham, Nagabhatla, Industrial & Engineering Chemistry Research, 2023, 62(4), 1788-1796

Production Method 4

496-11-7

581-42-0

3877-19-8

824-63-5

Reaction Conditions

1.1 Reagents: Hydrogen Solvents: Tetralin ;  3 h, 1 atm, 450 °C

Reference

Catalytic cracking of low-density polyethylene dissolved in various solvents: product distribution and coking behavior

Machhi, Dharmesh J.; et al, Journal of Material Cycles and Waste Management, 2023, 25(5), 3005-3020

Production Method 5

496-11-7

90-00-6

581-42-0

575-37-1

527-53-7

17059-52-8

Reaction Conditions

1.1 500 °C

Reference

Acetic acid conversion reactions on basic and acidic catalysts under biomass fast pyrolysis conditions

Psarras, A. C.; Michailof, C. M.; Iliopoulou, E. F.; Kalogiannis, K. G.; Lappas, A. A.; et al, Molecular Catalysis, 2019, 465, 33-42

Production Method 6

496-11-7

Reaction Conditions

1.1 Reagents: Butyllithium Solvents: Diethyl ether
1.2 -

Reference

The intermediate formation of [4]metacyclophane on flash vacuum thermolysis

Kostermans, Gerardus B. M.; et al, Journal of Organic Chemistry, 1988, 53(19), 4531-4

Production Method 7

496-11-7

575-37-1

629-62-9

Reaction Conditions

1.1 Catalysts: Iron ,  Calcium ;  15 min, 500 °C

Reference

Preparation of sodium silicate/red mud-based ZSM-5 with glucose as a second template for catalytic cracking of waste plastics into useful chemicals

Wang, Xiaofeng; et al, RSC Advances, 2022, 12(34), 22161-22174

Indane Raw materials

• Indane

Indane Preparation Products

• 1,3-DIETHYLBENZENE (141-93-5)
• 4'-Hydroxy-3'-methylacetophenone (876-02-8)
• 2-Ethylphenol (90-00-6)
• 2-Methoxy-4-methylphenol (93-51-6)
• Tridecane (629-50-5)
• 2,6-Dimethylnaphthalene (581-42-0)
• 3′,5′-Dimethoxyacetophenone (39151-19-4)
• 3,4,5-Trimethoxytoluene (6443-69-2)
• Indane (496-11-7)
• 1,7-Dimethylnaphthalene (575-37-1)
• n-Pentadecane (629-62-9)
• 1,3-Diisopropylbenzene (99-62-7)
• 1,2,3,5-Tetramethylbenzene (527-53-7)
• 1-tert-Butyl-2-methylbenzene (1074-92-6)
• Naphthalene,1,2,3,4-tetrahydro-2-methyl- (3877-19-8)
• 7-Methylbenzofuran (17059-52-8)
• Guaiacol (90-05-1)
• 1-Methyl-1H-indene (767-59-9)
• Benzene, 1,2-dipropyl- (17171-71-0)
• 1H-Indene,2,3-dihydro-2-methyl- (824-63-5)

• 1. Headspace solid-phase microextraction comprehensive 2D gas chromatography-time of flight mass spectrometry (HS-SPME-GC × GC-TOFMS) for origin traceability of the genus Hymenaea resinites
  Xiaopeng Su,Jing Yu,Zhaotong Shi,Yamei Wang,Yan Li RSC Adv. 2023 13 14150
• 2. Asymmetric α-alkylation of cyclic β-keto esters and β-keto amides by phase-transfer catalysis
  Yakun Wang,Yueyun Li,Mingming Lian,Jixia Zhang,Zhaomin Liu,Xiaofei Tang,Hang Yin,Qingwei Meng Org. Biomol. Chem. 2019 17 573
• 3. Facile access to functionalized indenes and fused quinolines by regioselective 5-enolexo-dig Michael addition and cyclization reactions
  Tohasib Yusub Chaudhari,Sandeep K. Ginotra,Vibha Tandon Org. Biomol. Chem. 2017 15 9319
• 4. Chemoenzymatic synthesis of enantiopure hydroxy sulfoxides derived from substituted arenes
  Derek R. Boyd,Narain D. Sharma,John F. Malone,Vera Ljubez,Deirdre Murphy,Steven D. Shepherd,Christopher C. R. Allen Org. Biomol. Chem. 2016 14 2651
• 5. Stereoselective synthesis and properties of 1,3-bis(dicyanomethylidene)indane-5-carboxylic acid acceptor fragment containing nonlinear optical chromophores
  Kaspars Traskovskis,Valdis Kokars,Andrejs Tokmakovs,Igors Mihailovs,Edgars Nitiss,Marina Petrova,Sergey Belyakov,Martins Rutkis J. Mater. Chem. C 2016 4 5019

• Solvents and Organic Chemicals Organic Compounds Benzenoids Indanes Indanes
• Solvents and Organic Chemicals Organic Compounds Benzenoids Indanes
• Solvents and Organic Chemicals Organic Compounds Hydrocarbons

• 6682-06-0(1H-Indene,2,3-dihydro-4,5,7-trimethyl-)
• 55282-70-7(1H-Indene,5,5'-(1,10-decanediyl)bis[2,3-dihydro-)
• 1076-17-1(as-Indacene,1,2,3,6,7,8-hexahydro-)
• 88632-75-1(1H-Indene, 5-ethyl-2,3-dihydro-4,7-dimethyl-)
• 874-35-1(5-Methylindan)
• 1206-79-7(2,3,4,5,6,7,8,9-Octahydro-1H-trindene)
• 824-22-6(4-Methylindan)
• 6682-71-9(1H-Indene,2,3-dihydro-4,7-dimethyl-)
• 1075-22-5(1H-Indene,2,3-dihydro-5,6-dimethyl-)
• 1685-82-1(1H-Indene,2,3-dihydro-4,6-dimethyl-)