9-Bromo-1-nonanol

Base Information

• Chemical Name: 9-Bromo-1-nonanol
• CAS No.: 55362-80-6
• Molecular Formula: C9H19BrO
• Molecular Weight: 223.153
• Hs Code.: 29055900
• European Community (EC) Number: 611-262-6,927-569-6
• DSSTox Substance ID: DTXSID8069016
• Nikkaji Number: J429.277D
• Wikidata: Q72448836
• Mol file: 55362-80-6.mol

Synonyms:9-Bromo-1-nonanol;9-bromononan-1-ol;55362-80-6;1-Nonanol, 9-bromo-;9-Bromo-nonan-1-ol;Nonamethylene bromohydrin;C9H19BrO;MFCD00063348;9-bromnonan-1-ol;9-bromononanol;9-Bromononyl alcohol;SCHEMBL99226;9-Bromo-1-nonanol, 95%;9-Bromo-1-nonanol, 97%;C9-H19-Br-O;DTXSID8069016;AMY4021;BCP12992;CS-B0284;STR06999;BBL103176;STL556986;AKOS015856511;AC-6708;9,9-Bis[4-(glycidyloxy)phenyl]fluorene;SY015344;B1785;FT-0663812;A25208;EN300-6740901;J-650011;J-650385;Q-200570

Chemical Property of 9-Bromo-1-nonanol

Chemical Property:

• Appearance/Colour: solid
• Vapor Pressure: 0.000545mmHg at 25°C
• Melting Point: 33-35 °C
• Refractive Index: 1.476
• Boiling Point: 277.8 °C at 760 mmHg
• PKA: 15.19±0.10(Predicted)
• Flash Point: 113.5 °C
• PSA: 20.23000
• Density: 1.188 g/cm³
• LogP: 3.10430
• Storage Temp.: −20°C
• Solubility.: Soluble in dichloromethane, ethyl acetate and hexane.
• XLogP3: 3.4
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 8
• Exact Mass: 222.06193
• Heavy Atom Count: 11
• Complexity: 66.6

Purity/Quality:

99% ^*data from raw suppliers

9-Bromononanol ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: C(CCCCO)CCCCBr
• Uses: 9-Bromo-1-nonanol is used as a pharmaceutical intermediate.

Technology Process of 9-Bromo-1-nonanol

There total 18 articles about 9-Bromo-1-nonanol which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 99.0%

(9-bromo-nonyloxy)-triethyl-silane → 9-bromononan-1-ol (55362-80-6)

Guidance literature:

With hydrogen; palladium on activated charcoal; In dichloromethane; at 20 ℃; for 0.0333333h; atmospheric pressure;

DOI:10.1016/j.tetlet.2003.12.145

Reference yield: 99.0%

(9-bromo-nonyloxy)-tripropyl-silane → 9-bromononan-1-ol (55362-80-6)

Guidance literature:

With hydrogen; palladium on activated charcoal; In dichloromethane; at 20 ℃; for 0.0333333h; atmospheric pressure;

DOI:10.1016/j.tetlet.2003.12.145

Reference yield: 99.0%

(9-bromo-nonyloxy)-tributyl-silane → 9-bromononan-1-ol (55362-80-6)

Guidance literature:

With hydrogen; palladium on activated charcoal; In dichloromethane; at 20 ℃; for 0.1h; atmospheric pressure;

DOI:10.1016/j.tetlet.2003.12.145

upstream raw materials:

1,9-Nonanediol

methyl 9-bromononanoate

9-bromononanoic acid

9-bromononyl acetate

Downstream raw materials:

(9'-Bromo-1'-nonyl)-3-oxobutanoate

9-bromononyl acetate

1-bromo-9-triphenylmethoxynonane

9-iodononan-1-ol

Refernces

• 1、 -. "Preparation method of (E,E,Z)-10, 12, 14-hexadecatriene acetate, composition and attractant core". Paragraph 0025; 0049-0051; 0061-0062. . Retrieved 2021/02/10.
• 2、 Elias, Marianne,Mann, Florian,McClure, Melanie,Schulz, Stefan,Silva, Lisa de,Szczerbowski, Daiane. "3-Acetoxy-fatty acid isoprenyl esters from androconia of the ithomiine butterfly Ithomia salapia". supporting information. p. 2776 - 2786. Retrieved 2020/12/29.