10-Bromodecanol

  • Name: 10-Bromodecanol
  • CAS: 53463-68-6
  • Purity: 99%
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Details

Quality Manufacturer Supply High Purity 99% 10-Bromodecanol 53463-68-6 with Reasonable Price

  • Molecular Formula: C10H21BrO
  • Molecular Weight: 237.18
  • Appearance/Colour: Clear yellow liquid 
  • Vapor Pressure: 0.000257mmHg at 25°C 
  • Refractive Index: n20/D 1.476(lit.)  
  • Boiling Point: 288.588 °C at 760 mmHg 
  • PKA: 15.20±0.10(Predicted) 
  • Flash Point: 118.313 °C 
  • PSA: 20.23000 
  • Density: 1.161 g/cm3 
  • LogP: 3.49440 

10-Bromodecanol(Cas 53463-68-6) Usage

InChI:InChI=1/C10H21BrO/c11-9-7-5-3-1-2-4-6-8-10-12/h12H,1-10H2

53463-68-6 Relevant articles

Hydroxyl-Assisted trans-Reduction of 1,3-Enynes: Application to the Formal Synthesis of (+)-Aspicilin

Schaubach, Sebastian,Michigami, Kenichi,Fürstner, Alois

, p. 202 - 208 (2017)

1,3-Enynes are hardly amenable to trans-...

Synthesis of ent-BE-43547A 1 reveals a potent hypoxia-selective anticancer agent and uncovers the biosynthetic origin of the APD-CLD natural products

Villadsen, Nikolaj L.,Jacobsen, Kristian M.,Keiding, Ulrik B.,Weibel, Esben T.,Christiansen, Bj?rn,Vosegaard, Thomas,Bjerring, Morten,Jensen, Frank,Johannsen, Mogens,T?rring, Thomas,Poulsen, Thomas B.

, p. 264 - 272 (2017)

Tumour hypoxia is speculated to be a key...

Improvement of antimalarial activity of a 3-alkylpiridine alkaloid analog by replacing the pyridine ring to a thiazole-containing heterocycle: Mode of action, mutagenicity profile, and Caco-2 cell-based permeability

Guimar?es, Daniel Silqueira Martins,de Sousa Luz, Letícia Silveira,do Nascimento, Sara Batista,Silva, Lorena Rabelo,de Miranda Martins, Natália Rezende,de Almeida, Heloísa Gon?alves,de Souza Reis, Vitória,Maluf, Sarah El Chamy,Budu, Alexandre,Marinho, Juliane Aparecida,Abramo, Clarice,Carmona, Adriana Karaoglanovic,da Silva, Marina Goulart,da Silva, Gisele Rodrigues,Kemmer, Victor Matheus,Butera, Anna Paola,Ribeiro-Viana, Renato Márcio,Gazarini, Marcos Leoni,Júnior, Clébio Soares Nascimento,Guimar?es, Luciana,dos Santos, Fabio Vieira,de Castro, Whocely Victor,Viana, Gustavo Henrique Ribeiro,de Brito, Cristiana Ferreira Alves,de Pilla Varotti, Fernando

, (2019)

The development of new antimalarial drug...

Toward the synthesis of the hypoxia selective anticancer agent BE-43547 A2

Kranthikumar, Ramagonolla

supporting information, p. 9833 - 9839 (2021/12/07)

A short and enantioselective synthesis o...

A New Asymmetric Synthesis of (S)-14-Methyloctadec-1-ene, the Sex Pheromone of the Peach Leafminer Moth

Bai, Hongjin,Du, Zhen-Ting,He, Guo-Guo,Liu, Lu,Tang, Meng,Wei, Liang,Zhang, Tao

, p. 1089 - 1095 (2020/07/25)

Abstract: An asymmetric synthesis of 14-...

Synthesis method of sex pheromone (S)-14-methyl-1-octadecene of lepidoptera pest peach leaf miners

-

Paragraph 0047; 0065-0066, (2020/08/02)

The invention discloses a synthesis meth...

Industrial synthesis method of dichocrocis punctiferalis sex pheromone

-

Paragraph 0023-0025, (2020/06/30)

The invention belongs to the field of ch...

53463-68-6 Process route

1,10-Decanediol
112-47-0

1,10-Decanediol

1-bromo-10-decanol
53463-68-6

1-bromo-10-decanol

1,10-dibromodecane
4101-68-2

1,10-dibromodecane

Conditions
Conditions Yield
With hydrogen bromide; In cyclohexane; for 6h; Heating;
9%
88%
With hydrogen bromide; In toluene; for 48h; Heating;
87%
With hydrogen bromide; In water; toluene; Reflux;
87%
With hydrogen bromide;
73%
With tetrabutylammomium bromide; hydrogen bromide; In water; at 105 ℃; for 2h; chemoselective reaction;
64%
10%
With tetrabutylammomium bromide; hydrogen bromide; In water; at 100 ℃; for 0.0833333h; Microwave irradiation;
45%
With hydrogen bromide; at 130 ℃;
With hydrogen bromide; In para-xylene; water; at 130 - 135 ℃; for 6.5h; Dean-Stark;
1,10-Decanediol
112-47-0

1,10-Decanediol

1-bromo-10-decanol
53463-68-6

1-bromo-10-decanol

Conditions
Conditions Yield
With hydrogen bromide; In water; toluene; for 16h; Inert atmosphere; Reflux; Dean-Stark;
93%
With hydrogen bromide; In water; toluene; Reflux; Inert atmosphere;
92%
With hydrogen bromide; In water; toluene; Reflux;
92%
With hydrogen bromide; In toluene; at 180 ℃; for 24h;
92%
With hydrogen bromide; In water; toluene; for 72h; Heating / reflux;
90%
With hydrogen bromide; In water; toluene; for 72h; Heating / reflux;
90%
With hydrogen bromide; In toluene; for 16h; Heating;
89%
With hydrogen bromide; In cyclohexane; water; for 6h; Heating / reflux;
89%
With hydrogen bromide; In toluene; for 24h; Reflux;
88.93%
With hydrogen bromide; In toluene; Reflux;
88.18%
With hydrogen bromide; In water; Petroleum ether; for 4h; Heating / reflux;
87%
With hydrogen bromide; In benzene; for 28h; Heating;
85%
With hydrogen bromide; In toluene;
85%
With hydrogen bromide; In toluene; for 72h; Reflux; Inert atmosphere;
84%
With hydrogen bromide; In toluene; at 110 ℃; for 24h;
84%
With hydrogen bromide; In water; toluene; at 95 - 97 ℃; for 72h;
82%
With hydrogen bromide; In water; toluene; for 48h; Reflux; Inert atmosphere;
82%
With hydrogen bromide;
81%
With hydrogen bromide; In benzene; for 30h; Heating;
80%
With hydrogen bromide; In benzene; for 28h; Heating;
80%
With hydrogen bromide; In benzene; Heating;
80%
With tetrabutylammomium bromide; hydrogen bromide; In water; for 0.0833333h; Microwave irradiation;
80%
With hydrogen bromide; tetra-(n-butyl)ammonium iodide; In water; for 0.0833333h; Microwave irradiation;
80%
With hydrogen bromide; In water; toluene; for 43h; Inert atmosphere; Reflux;
79%
With hydrogen bromide; at 85 ℃; for 3h;
78%
With hydrogen bromide;
78%
With hydrogen bromide; In cyclohexane; water; at 80 ℃; for 5h; Inert atmosphere;
78.5%
With hydrogen bromide; In water; toluene; for 6h; Reflux;
77%
With hydrogen bromide; at 70 ℃; for 40h;
74%
With hydrogen bromide; In water; toluene; for 36h; Reflux;
74.5%
With hydrogen bromide; In water; toluene; for 48h; Reflux;
74%
With hydrogen bromide; In water; toluene; for 16h; Dean-Stark; Reflux;
74%
With hydrogen bromide; In water; toluene; for 16h; Reflux;
73%
With hydrogen bromide; In n-heptane;
70%
With hydrogen bromide; In n-heptane; for 25h; Heating;
70%
With hydrogen bromide;
69%
In hydrogen bromide;
69%
With hydrogen bromide; In toluene; Heating;
68%
With hydrogen bromide; In ligroin; for 72h;
67.1%
With hydrogen bromide; In Petroleum ether; at 90 - 95 ℃; for 65h;
65%
With hydrogen bromide; In benzene; for 24h; Heating;
63%
With hydrogen bromide; In toluene; at 20 ℃; for 18h;
59%
With hydrogen bromide; In water; toluene; for 48h; Reflux; Inert atmosphere;
57%
With hydrogen bromide; In water; toluene; Reflux; Dean-Stark;
57%
With hydrogen bromide; In water; toluene; at 90 - 95 ℃; for 48h;
56%
With hydrogen bromide;
48%
With water; hydrogen bromide;
With hydrogen bromide; In n-heptane; Heating;
With hydrogen bromide; In Petroleum ether;
With hydrogen bromide; In toluene;
With hydrogen bromide; In water; for 60h; Heating;
With sulfuric acid; hydrogen bromide; for 2h; Heating;
With hydrogen bromide; In n-heptane; Heating;
With hydrogen bromide; In cyclohexane; for 6h; Heating;
With hydrogen bromide; In toluene; for 72h; Heating;
With hydrogen bromide; In cyclohexane; for 6h; Heating;
In hexane; hydrogen bromide;
In hexane; hydrogen bromide;
With hydrogen bromide; In toluene; for 16h; Reflux;
With hydrogen bromide; In benzene; for 2.5h; Reflux;
73.47 mg
With hydrogen bromide; In toluene; for 75h; Reflux;
With hydrogen bromide; In toluene; at 120 ℃; for 16h;
With hydrogen bromide; In water; toluene; for 48h; Reflux;

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