20194-45-0

Basic information

• Product Name: 10-Methylundecanol
• Synonyms: 10-Methylundecanol;10-Methyl-1-undecanol
• CAS NO: 20194-45-0
• Molecular Formula: C₁₂H₂₆O
• Molecular Weight: 186.33424
• Product Categories: Aliphatics;Intermediates;Intermediates & Fine Chemicals;Pharmaceuticals
• Mol File: 20194-45-0.mol
• Article Data: 10

Chemical Properties

• Melting Point: 16.85°C (estimate)
• Boiling Point: 250.85°C (estimate)
• Appearance: /
• Density: 0.8429 (estimate)
• Refractive Index: 1.4162 (estimate)
• Storage Temp.: Refrigerator
• Solubility: Chloroform (Slightly), Methanol (Slightly)
• CAS DataBase Reference: 10-Methylundecanol(CAS DataBase Reference)
• NIST Chemistry Reference: 10-Methylundecanol(20194-45-0)
• EPA Substance Registry System: 10-Methylundecanol(20194-45-0)

Safety Data

• Hazardous Substances Data: 20194-45-0(Hazardous Substances Data)

Usage

Uses

10-Methylundecanol is an intermediate in the synthesis of Sulfobacin A.

Upstream product

• 2724-56-3 isolauric acid 
• 124388-94-9 10-methyl-1-tetrahydro-2H-pyran-2-yloxyundecane 
• 333335-25-4 10-Methyl-undec-9-en-1-ol 
• 50816-20-1 2-(8-bromooctyloxy)tetrahydropyran 
• 926-62-5 isobutylmagnesium bromide 
• 5129-56-6 undecanoic acid, 10-methyl-, methyl ester 
• 626-88-0 1-bromo-5-methylpentane 
• 50530-06-8 6-bromohexanoic acid sodium salt 
• 18993-09-4 methyl 10-oxoundecanoate 
• 219617-24-0 methyl 10-methylundec-10-enoate 
• 111-81-9 Methyl 10-undecenoate 
• 54704-39-1 (+/-)-10-Hydroxyundecansaeure-methylester 
• 176248-72-9 methyl 10-(tosyloxy)undecanoate 
• 51326-52-4 8-(tetrahydro-2H-pyran-2-yloxy)octan-1-ol 

Downstream Products

• 68820-37-1 10-methylundecan-1-al 
• 124388-95-0 1-bromo-10-methylundecane 
• 2724-56-3 isolauric acid 
• 942137-21-5 C₂₅H₄₂O₂ 
• 942137-22-6 C₂₅H₄₂O 
• 1560-89-0 2-methylheptadecane 
• 22370-55-4 10-methylundec-1-ene 
• 148915-78-0 isolauryl 5-hydroxyanthranilate 

Relevant articles and documents

Identification and total synthesis of novel fatty acids from the siphonarid limpet Siphonaria denticulata

The novel fatty acids 17-methyl-6(Z)-octadecenoic acid and 17-methyl-7(Z)-octadecenoic acid were identified for the first time in nature in the mollusk Siphonaria denticulata from Queensland, Australia. The principal fatty acids in the limpet were hexadecanoic acid, octadecanoic acid, and (Z)-9-octadecenoic acid, while the most interesting series of monounsaturated fatty acids was a family of five nonadecenoic acids with double bonds at either Δ7, Δ9, Δ12, or Δ13. The novel compounds were characterized using a combination of GC-MS and chemical transformations, such as dimethyl disulfide derivatization. The first total syntheses for the two novel methyl-branched nonadecenoic acids are also described, and these were accomplished in four to five steps and in high yields.

Structural and Functional Analysis of Bacterial Sulfonosphingolipids and Rosette-Inducing Factor 2 (RIF-2) by Mass Spectrometry-Guided Isolation and Total Synthesis

We have analyzed the abundance of bacterial sulfonosphingolipids, including rosette-inducing factors (RIFs), in seven bacterial prey strains by using high-resolution tandem mass spectrometry (HRMS2) and molecular networking (MN) within the Glob

An asymmetric synthesis of sulfobacin A

A facile synthesis of sulfobacin A has been developed starting from (R)-cyclohexylideneglyceraldehyde (11). The key steps in the synthesis are the highly diastereocontrolled allylation of 11 and syn-selective reduction of a ketone derived from 11. The oth