Production Method 1

34036-07-2

85118-05-4

Reaction Conditions

1.1 Reagents: Sodium borohydride Solvents: Methanol

Reference

Synthesis, inhibition properties against xanthine oxidase and molecular docking studies of dimethyl N-benzyl-1H-1,2,3-triazole-4,5-dicarboxylate and (N-benzyl-1H-1,2,3-triazole-4,5-diyl)dimethanol derivatives

Yagiz, Guler; Noma, Samir Abbas Ali; Altundas, Aliye; Al-khafaji, Khattab; Taskin-Tok, Tugba; et al, Bioorganic Chemistry, 2021, 108,

Production Method 2

34036-07-2

85118-05-4

Reaction Conditions

1.1 Reagents: Sodium borohydride Solvents: Methanol ;  0 °C; 30 min, 0 °C

Reference

Tetramethoxystilbene Inhibits NLRP3 Inflammasome Assembly via Blocking the Oligomerization of Apoptosis-Associated Speck-like Protein Containing Caspase Recruitment Domain: In Vitro and In Vivo Evaluation

Abdullaha, Mohd; Ali, Mehboob; Kour, Dilpreet; Mudududdla, Ramesh; Khajuria, Parul; et al, ACS Pharmacology & Translational Science, 2021, 4(4), 1437-1448

Production Method 3

34036-07-2

85118-05-4

Reaction Conditions

1.1 Reagents: Zinc ,  Ammonium chloride Solvents: Tetrahydrofuran ,  Water ;  20 min, rt

Reference

Zinc-Mediated Efficient and Selective Reduction of Carbonyl Compounds

Mandal, Tirtha; Jana, Snehasish; Dash, Jyotirmayee, European Journal of Organic Chemistry, 2017, 2017(33), 4972-4983

Production Method 4

34036-07-2

85118-05-4

Reaction Conditions

1.1 Reagents: Sodium borohydride Solvents: Methanol ;  0 °C; 2 h, rt
1.2 Reagents: Hydrochloric acid Solvents: Water

Reference

Synthesis of structurally diverse diarylketones through the diarylmethyl sp3 C-H oxidation

He, Chao; Zhang, Xiaohui; Huang, Ruofeng; Pan, Jing; Li, Jiaqiang; et al, Tetrahedron Letters, 2014, 55(32), 4458-4462

Production Method 5

369-25-5

85118-05-4

Reaction Conditions

1.1 Reagents: Hydrogen ,  Sodium borohydride Catalysts: 2088430-88-8 Solvents: Tetrahydrofuran ;  24 h, 5 MPa, 120 °C

Reference

Cooperative interplay between a flexible PNN-Ru(II) complex and a NaBH4 additive in the efficient catalytic hydrogenation of esters

Wang, Zheng; Chen, Xiangyang; Liu, Bo; Liu, Qing-bin; Solan, Gregory A.; et al, Catalysis Science & Technology, 2017, 7(6), 1297-1304

(3,4-difluorophenyl)methanol Raw materials

• 3,4-Difluorobenzaldehyde
• Methyl 3,4-difluorobenzoate

(3,4-difluorophenyl)methanol Preparation Products

• (3,4-difluorophenyl)methanol (85118-05-4)

• 1. Fate of Sb(v) and Sb(iii) species along a gradient of pH and oxygen concentration in the Carnoulès mine waters (Southern France)
  Eléonore Resongles,Corinne Casiot,Fran?oise Elbaz-Poulichet,Rémi Freydier,Odile Bruneel,Christine Piot,Sophie Delpoux,Aurélie Volant,Angélique Desoeuvre Environ. Sci.: Processes Impacts, 2013,15, 1536-1544
• 2. Dissolved oxygen sensor based on fluorescence quenching of oxygen-sensitive ruthenium complexes immobilized in sol–gel-derived porous silica coatings
  Analyst, 1996,121, 785-788
• 3. Enabling shape memory and healable effects in a conjugated polymer by incorporating siloxane via dynamic imine bond?
  Yaling Zhang,Chunhui Dai,Shiwei Zhou,Bin Liu Chem. Commun., 2018,54, 10092-10095
• 4. Excimer formation effects and trap-assisted charge recombination loss channels in organic solar cells of perylene diimide dimer acceptors?
  Min Kim,Jae-Joon Lee,Tengling Ye,Panagiotis E. Keivanidis,Kilwon Cho J. Mater. Chem. C, 2020,8, 1686-1696
• 5. Emerging investigator series: heterogeneous reactions of sulfur dioxide on mineral dust nanoparticles: from single component to mixed components?
  Tao Wang,Yangyang Liu,Yue Deng,Hongbo Fu,Jianmin Chen Environ. Sci.: Nano, 2018,5, 1821-1833

• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Benzyl alcohols
• Solvents and Organic Chemicals Organic Compounds Alcohol/Ether

• 456-47-3(3-Fluorobenzyl alcohol)
• 75853-18-8(2,3-Difluorobenzyl alcohol)
• 114152-19-1(2,3,6-Trifluorobenzyl Alcohol)
• 144284-24-2(2,3,4-Trifluorobenzyl Alcohol)
• 67640-33-9(2,3,5-Trifluorobenzyl Alcohol)
• 79538-03-7(2,3,5,6-Tetrafluoro-4-methylbenzyl Alcohol)
• 79538-20-8((3,5-difluorophenyl)methanol)
• 144284-25-3(2,4,5-Trifluorobenzyl alcohol)
• 4084-38-2(2,3,5,6-Tetrafluorobenzyl alcohol)
• 459-56-3(4-Fluorobenzyl Alcohol)