Methyl Tetracosanoate

• CAS: 2442-49-1
• Catalog Number: ALC-FP-2442491
• Category: Other Products; Fatty Acids and Ester Homologs
• Molecular Weight: 382.66
• Molecular Formula: C25H50O2
• Synonyms: Lignoceric Acid Methyl Ester
• Canonical SMILES: CCCCCCCCCCCCCCCCCCCCCCCC(=O)OC
• Boiling Point: 232 °C (lit.) at 4 mmHg
• Melting Point: 58-60 °C (lit.)
• Appearance: Powder
• Storage: Room temperature
• CNo.Chain: C24:0
• Compound Derivative: Methyl
• Fatty Aci: Tetracosanoic; (Lignoceric)
• Physical State: Solid

Synthetic Use

Upstream Synthesis Route 1

• 67-56-1
• 8001-22-7

• 14663-11-7
• 88400-02-6
• 10030-74-7
• 112-62-9
• 112-63-0
• 1120-34-9
• 2733-88-2
• 124-10-7
• 112-39-0
• 1731-92-6
• 112-61-8
• 1120-28-1
• 929-77-1
• 2442-49-1
• 10305-59-6
• 37929-05-8
• 56-81-5

Reference: [1] Patent: WO2007/12190, 2007, A1, . Location in patent: Page/Page column 16-18

Upstream Synthesis Route 2

• 67-56-1

• 14663-11-7
• 88400-02-6
• 10030-74-7
• 112-62-9
• 112-63-0
• 1120-34-9
• 2733-88-2
• 124-10-7
• 112-39-0
• 1731-92-6
• 112-61-8
• 1120-28-1
• 929-77-1
• 2442-49-1
• 10305-59-6
• 37929-05-8
• 56-81-5

Reference: [1] Patent: WO2007/12190, 2007, A1, . Location in patent: Page/Page column 13-15

Upstream Synthesis Route 3

• 67-56-1

• 14663-11-7
• 88400-02-6
• 10030-74-7
• 112-62-9
• 112-63-0
• 1120-34-9
• 2733-88-2
• 124-10-7
• 112-39-0
• 1731-92-6
• 112-61-8
• 1120-28-1
• 929-77-1
• 2442-49-1
• 10305-59-6
• 37929-05-8
• 56-81-5

Reference: [1] Patent: WO2007/12190, 2007, A1, . Location in patent: Page/Page column 10-12

Upstream Synthesis Route 4

• 557-59-5

• 2442-49-1

Reference: [1]Bhatt,S.
[Indian Journal of Chemistry, 1975, vol. 13, p. 1105 - 1108]
[2]Rama Rao, A. V.; Deshmukh, M. N.; Kamalam, M.
[Tetrahedron, 1981, vol. 37, p. 227 - 230]

Upstream Synthesis Route 5

• 929-33-9
• 117711-00-9

• 2442-49-1

Reference: [1]Gensler,W.J. et al.
[Tetrahedron, 1979, vol. 35, p. 2595 - 2600]

Downstream Synthesis Route 1

• 2442-49-1

• 506-51-4

Reference: [1]Gensler,W.J. et al.
[Tetrahedron, 1979, vol. 35, p. 2595 - 2600]
[2]Rao, S. Jagadishwar; Bhalerao, U. T.; Tilak, B. D.
[Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 1987, vol. 26, # 1-12, p. 208 - 211]

* For details of the synthesis route, please refer to the original source to ensure accuracy.