10-Bromodecanal

Base Information

• Chemical Name: 10-Bromodecanal
• CAS No.: 85920-81-6
• Molecular Formula: C10H19BrO
• Molecular Weight: 235.164
• Hs Code.: 2913000090
• DSSTox Substance ID: DTXSID00448882
• Wikidata: Q82268074
• Mol file: 85920-81-6.mol

Synonyms:10-bromodecanal;85920-81-6;10-bromo-1-decanal;Decanal, 10-bromo-;C10H19BrO;SCHEMBL4725387;DTXSID00448882;JRVIFIREWVQSDU-UHFFFAOYSA-N;AKOS016006313;MS-21716

Chemical Property of 10-Bromodecanal

Chemical Property:

• Boiling Point: 282.237 °C at 760 mmHg
• Flash Point: 27.016 °C
• PSA: 17.07000
• Density: 1.152 g/cm³
• LogP: 3.70100
• Storage Temp.: 2-8°C
• XLogP3: 4.1
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 9
• Exact Mass: 234.06193
• Heavy Atom Count: 12
• Complexity: 93.8

Purity/Quality:

99% ^*data from raw suppliers

10-Bromodecanal 95+% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C(CCCCC=O)CCCCBr

Technology Process of 10-Bromodecanal

There total 11 articles about 10-Bromodecanal 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%

1-bromo-10-decanol (53463-68-6) → 10-bromodecanal (85920-81-6)

Guidance literature:

With pyridinium chlorochromate; In dichloromethane; for 3h; Ambient temperature;

Reference yield: 55.0%

→ 10-bromodecanal (85920-81-6)

Guidance literature:

With pyridinium chlorochromate; In dichloromethane; at 15 ℃;

Reference yield:

1-undecen-11-ylbromide (7766-50-9) → 10-bromodecanal (85920-81-6) + 10-bromodecanoic acid (50530-12-6)

Guidance literature:

With tetrachloromethane; water; bei der Ozonspaltung;

upstream raw materials:

1-undecen-11-ylbromide

1-bromo-10-decanol

1,10-Decanediol

10-Undecen-1-ol

Downstream raw materials:

10-bromodecanoic acid

C₃₀H₄₈I₂O₆

(15S,16S)-Penaresidin A

(2S,3R,4S)-2-Hydroxymethyl-4-((11S,12S)-11-hydroxy-12-methyl-tetradecyl)-1-(toluene-4-sulfonyl)-azetidin-3-ol

Refernces

• 1、 -. "IONIZABLE AMINE LIPIDS". Page/Page column 69-70; 72. . Retrieved 2020/05/15.
• 2、 Kunkalkar, Rupesh A.,Fernandes, Rodney A.. "Protecting-Group-Free Total Synthesis of Chatenaytrienin-2". . p. 12216 - 12220. Retrieved 2019/10/11.