9,10-dibromodecan-1-ol

Base Information

• Chemical Name: 9,10-dibromodecan-1-ol
• CAS No.: 114838-32-3
• Molecular Formula: C10H20 Br2 O
• Molecular Weight: 316.076
• Mol file: 114838-32-3.mol

Synonyms:9,10-Dibromodecan-1-ol

Chemical Property of 9,10-dibromodecan-1-ol

Chemical Property:

• Vapor Pressure: 5.84E-06mmHg at 25°C
• Boiling Point: 340.1°C at 760 mmHg
• Flash Point: 159.5°C
• Density: 1.45g/cm³

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of 9,10-dibromodecan-1-ol

There total 2 articles about 9,10-dibromodecan-1-ol 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: 100.0%

9-Decen-1-ol (13019-22-2) → 9,10-dibromodecan-1-ol (114838-32-3)

Guidance literature:

With bromine; In dichloromethane; at -45 - 20 ℃;

DOI:10.1021/ja1050742

Reference yield:

→ 9,10-dibromodecan-1-ol (114838-32-3)

Guidance literature:

In dichloromethane; at 0 - 20 ℃;

Reference yield: 72.0%

9,10-dibromodecan-1-ol (114838-32-3) + 2,4,6-trimethylaniline (88-05-1) → C28H44N2O (1436389-62-6)

Guidance literature:

9,10-dibromodecan-1-ol; 2,4,6-trimethylaniline; at 125 ℃; for 24h;

With sodium hydroxide; at 20 ℃;

DOI:10.1039/c3dt33010a

upstream raw materials:

9-Decen-1-ol

Downstream raw materials:

9-decyn-1-ol

2-dec-9-ynyloxy-tetrahydro-pyran

dec-9-ynoic acid

Benzoic acid (2E,4Z)-(R)-13-hydroxy-1-pentyl-trideca-2,4-dienyl ester

Refernces

• 1、 -. "Maltoside and Phosphocholine Derivatives, Uses thereof and Methods of Preparing Artificial Lipid Structures Thereof". Paragraph 0055. . Retrieved 2013/04/24.
• 2、 Meyer, Matthew P.,Klinman, Judith P.. "Synthesis of linoleic acids combinatorially labeled at the vinylic positions as substrates for lipoxygenases". . p. 3600 - 3603. Retrieved 2008/09/19.