Production Method 1

32281-97-3

91270-69-8

Reaction Conditions

1.1 Reagents: 2,4,6-Trimethylpyridine ,  Triisopropylsilyl triflate Catalysts: (OC-6-42)-Bis[[2,3-butanedione 2,3-di(oximato-κN)](1-)]chloro(N,N-dimethyl-4-pyr… ,  Iridium(1+), [4,4′-bis(trifluoromethyl)-2,2′-bipyridine-κN1,κN1′]bis[3-fluoro-5-… Solvents: Dichloromethane ,  1,2-Dichloroethane ;  10 h, rt
1.2 Reagents: Tetrabutylammonium fluoride Solvents: Tetrahydrofuran ;  20 min, rt

Reference

Rapid Access to Free Phenols by Photocatalytic Acceptorless Dehydrogenation of Cyclohexanones at Room Temperature

Min, Lin; Lin, Jiani; Shu, Wei, Chinese Journal of Chemistry, 2023, 41(21), 2773-2778

Production Method 2

580-13-2

91270-69-8

771-15-3

90767-17-2

Reaction Conditions

1.1 Reagents: m-Chloroperbenzoic acid Catalysts: Manganese(1+), [5,10,15,20-tetrakis(pentafluorophenyl)-21H,23H-porphinato(2-)-κN… Solvents: Acetonitrile ,  Dichloromethane ;  1 h, rt; 27 °C

Reference

Substituent-induced regioselective hydroxylation of the aromatic C-H bond on naphthalene with metachloroperbenzoic acid catalyzed by F20TPPMnCl

Chen, Chang-Di; Sheng, Wen-Bing; Shi, Guo-Jun; Guo, Can-Cheng, Journal of Physical Organic Chemistry, 2013, 26(1), 23-29

Production Method 3

174814-12-1

91270-69-8

Reaction Conditions

1.1 Reagents: Perchloric acid Solvents: Acetonitrile ;  rt

Reference

Acid-Catalyzed Dehydration of Naphthalene-cis-1,2-dihydrodiols: Origin of Impaired Resonance Effect of 3-Substituents

Kudavalli, Jaya Satyanarayana; Boyd, Derek R.; Sharma, Narain D.; More O'Ferrall, Rory A., Journal of Organic Chemistry, 2011, 76(22), 9338-9343

Production Method 4

91270-69-8

Reaction Conditions

Reference

Arynic species: effect of substituents on the reactivity of monosubstituted dehydrobenzenes

Gavina, F.; Luis, S. V.; Costero, A. M.; Gil, P., Tetrahedron, 1986, 42(1), 155-66

Production Method 5

110138-21-1

26447-28-9

91270-69-8

91270-68-7

Reaction Conditions

1.1 Solvents: 1,4-Dioxane

Reference

Arynic species. II. Tosyl and triazene as leaving group in the generation of arynes from polymer-bound reagents

Gavina, F.; Luis, S. V.; Ferrer, P.; Costero, A. M.; Gil, P., Tetrahedron, 1986, 42(20), 5641-8

Production Method 6

148378-71-6

91270-69-8

Reaction Conditions

1.1 Reagents: Triethylamine Catalysts: Palladium diacetate ,  1,1′-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis[1,1-diphenylphosphine] Solvents: 1,2-Dichloroethane ;  rt → 70 °C; 18 h, 70 °C

Reference

Total Synthesis of Elmenols A and B and Related Rearranged Angucyclinones

Ikonnikova, Viktoria A. ; Solyev, Pavel N. ; Terekhov, Stanislav S.; Alferova, Vera A.; Tyurin, Anton P.; et al, ChemistrySelect, 2021, 6(42), 11775-11778

Production Method 7

477907-60-1

91270-69-8

Reaction Conditions

1.1 Reagents: Hydrochloric acid Solvents: Ethanol ;  20 h, 50 °C

Reference

Substituted 9-Diethylaminobenzo[a]phenoxazin-5-ones (Nile Red Analogues): Synthesis and Photophysical Properties

Hornum, Mick ; Mulberg, Mads W.; Szomek, Maria; Reinholdt, Peter ; Brewer, Jonathan R. ; et al, Journal of Organic Chemistry, 2021, 86(2), 1471-1488

Production Method 8

91270-69-8

Reaction Conditions

Reference

New chiral synthons from the microbial oxidation of bromonaphthalenes

Hudlicky, Tomas; Endoma, Mary Ann A.; Butora, Gabor, Tetrahedron: Asymmetry, 1996, 7(1), 61-8

7-Bromonaphthalen-1-ol Raw materials

• BENZOIC ACID, 5-BROMO-2-(1-TRIAZENYL)-
• Furancarboxylic acid
• 7-Bromo-1-tetralone
• 2-Bromonaphthalene
• 1,2-Naphthalenediol, 7-bromo-1,2-dihydro-, (1R,2S)-
• 2,7-Dibromo-3,4-dihydronaphthalen-1(2H)-one
• 4-bromo-11-oxatricyclo6.2.1.0,2,7undeca-2,4,6,9-tetraene

7-Bromonaphthalen-1-ol Preparation Products

• 6-bromonaphthalen-1-ol (91270-68-7)
• 2-Bromonaphthalen-1-ol (771-15-3)
• 3-Bromonaphthalen-1-ol (90767-17-2)
• 7-Bromonaphthalen-1-ol (91270-69-8)

• 1. An amorphous carbon nitride/NiO/CoN-based composite: a highly efficient nonprecious electrode for supercapacitors and the oxygen evolution reaction?
  Huifang Yang,Haoran Guo,Peidong Fan,Xinpan Li,Wenlu Ren,Rui Song Nanoscale, 2020,12, 7024-7034
• 2. An approach to the structure and vibrational analysis of cis- and trans-3-chlorostyrene through IR/Raman and INS spectroscopies and theoretical ab initio/DFT calculations?
  J. M. Granadino-Roldán,M. Fernández-Gómez,A. Navarro,T. Pe?a Ruiz,U. A. Jayasooriya Phys. Chem. Chem. Phys., 2004,6, 1133-1143
• 3. An aptamer-based keypad lock system?
  Yaqing Liu,Jiangtao Ren,Jing Li,Jiyang Liu,Erkang Wang Chem. Commun., 2012,48, 802-804
• 4. An autonomous self-optimizing flow machine for the synthesis of pyridine–oxazoline (PyOX) ligands?
  Eric Wimmer,Daniel Cortés-Borda,Solène Brochard,Elvina Barré,Charlotte Truchet,Fran?ois-Xavier Felpin React. Chem. Eng., 2019,4, 1608-1615
• 5. An apparatus for testing water by measurement of its electrical conductivity
  Analyst, 1912,37, 538-543

• Solvents and Organic Chemicals Organic Compounds Benzenoids Naphthalenes Naphthols and derivatives

• 52927-23-8(5-Bromonaphthalen-1-OL)
• 571-57-3(4-Bromonaphthalen-1-ol)
• 50457-15-3(6-bromonaphthalene-1,2-diol)
• 91270-68-7(6-bromonaphthalen-1-ol)
• 7385-87-7(8-Bromo-2-naphthol)
• 62456-32-0(8-Bromonaphthalen-1-ol)
• 114562-65-1(6-BROMO-1-HYDROXYPYRENE)
• 116230-30-9(7-Bromonaphthalen-2-ol)
• 15231-91-1(6-bromonaphthalen-2-ol)
• 116632-05-4(5-Bromo-2-naphthalenol)