Trimorpholinophosphine oxide

• CAS: 4441-12-7
• Catalog Number: ACM4441127
• Category: Organic Phosphine Compounds
• Molecular Weight: 305.31
• Molecular Formula: C₁₂H₂₄N₃O₄P
• Synonyms: Phosphoric Trimorpholide; 4-dimorpholin-4-ylphosphorylmorpholine; Trimorpholinophosphine Oxide; Phosphoric acid trimorpholide
• IUPAC Name: 4-dimorpholin-4-ylphosphorylmorpholine
• Canonical SMILES: C1COCCN1P(=O)(N2CCOCC2)N3CCOCC3
• InChI Key: WXMQHPKQCPCDQO-UHFFFAOYSA-N
• Boiling Point: 476.4ºC at 760 mmHg
• Melting Point: 188-192ºC
• Flash Point: 241.9ºC
• Density: 1.3 g/cm³
• EC Number: 224-662-7
• Exact Mass: 305.15000
• Safety Description: S26-S36

Custom Q&A

What is the molecular formula of Trimorpholinophosphine oxide?

The molecular formula of Trimorpholinophosphine oxide is C12H24N3O4P.

What is the molecular weight of Trimorpholinophosphine oxide?

The molecular weight of Trimorpholinophosphine oxide is 305.31 g/mol.

What is the IUPAC name of Trimorpholinophosphine oxide?

The IUPAC name of Trimorpholinophosphine oxide is 4-dimorpholin-4-ylphosphorylmorpholine.

What is the InChI of Trimorpholinophosphine oxide?

The InChI of Trimorpholinophosphine oxide is InChI=1S/C12H24N3O4P/c16-20(13-1-7-17-8-2-13,14-3-9-18-10-4-14)15-5-11-19-12-6-15/h1-12H2.

What is the InChIKey of Trimorpholinophosphine oxide?

The InChIKey of Trimorpholinophosphine oxide is WXMQHPKQCPCDQO-UHFFFAOYSA-N.

What is the canonical SMILES of Trimorpholinophosphine oxide?

The canonical SMILES of Trimorpholinophosphine oxide is C1COCCN1P(=O)(N2CCOCC2)N3CCOCC3.

What is the CAS number of Trimorpholinophosphine oxide?

The CAS number of Trimorpholinophosphine oxide is 4441-12-7.

What is the UNII of Trimorpholinophosphine oxide?

The UNII of Trimorpholinophosphine oxide is K6FWD4S4ZD.

How many hydrogen bond acceptor count does Trimorpholinophosphine oxide have?

Trimorpholinophosphine oxide has 7 hydrogen bond acceptor count.

Synthetic Use

Upstream Synthesis Route 1

• 110-91-8

• 4441-12-7

Reference: [1] Journal of the American Chemical Society, 1942, vol. 64, p. 1553
[2] Farmaco, Edizione Scientifica, 1955, vol. 10, p. 15,19
[3] Journal of Coordination Chemistry, 2017, vol. 70, # 7, p. 1285 - 1302
[4] Monatshefte fur Chemie, 2018, vol. 149, # 10, p. 1759 - 1776
[5] Patent: DE1005963, 1955, ,

Upstream Synthesis Route 2

• 110-91-8
• 824-72-6

• 4441-12-7

Reference: [1] Journal of Coordination Chemistry, 2013, vol. 66, # 15, p. 2647 - 2658

Upstream Synthesis Route 3

• 22630-09-7

• 4441-12-7

Reference: [1] J. Gen. Chem. USSR (Engl. Transl.), 1984, vol. 54, # 7, p. 1336 - 1340[2] Zhurnal Obshchei Khimii, 1984, vol. 54, # 7, p. 1499 - 1503

Upstream Synthesis Route 4

• 110-91-8

• 4441-12-7

Reference: [1]Audrieth; Toy
[Journal of the American Chemical Society, 1942, vol. 64, p. 1553]
Malatesta; Tarantino
[Farmaco, Edizione Scientifica, 1955, vol. 10, p. 15,19]
[2]Pourayoubi, Mehrdad; Tarahhomi, Atekeh; Golen, James A.; Rheingold, Arnold L.
[Journal of Coordination Chemistry, 2017, vol. 70, # 7, p. 1285 - 1302]
[3]Tarahhomi, Atekeh; van der Lee, Arie
[Monatshefte fur Chemie, 2018, vol. 149, # 10, p. 1759 - 1776]
[4]Current Patent Assignee: EVONIK INDUSTRIES AG - DE1005963, 1955, B

Upstream Synthesis Route 5

• 22630-09-7

• 4441-12-7

Reference: [1]Shevchenko, M. V.; Kukhar', V. P.
[Journal of general chemistry of the USSR, 1984, vol. 54, # 7, p. 1336 - 1340][Zhurnal Obshchei Khimii, 1984, vol. 54, # 7, p. 1499 - 1503]

Upstream Synthesis Route 6

• 22630-09-7
• 7264-90-6

• 4441-12-7

Reference: [1]Shevchenko, M. V.; Kukhar', V. P.
[Journal of general chemistry of the USSR, 1984, vol. 54, # 7, p. 1336 - 1340][Zhurnal Obshchei Khimii, 1984, vol. 54, # 7, p. 1499 - 1503]