Diethyl carbamoylmethylphosphonate

• CAS: 5464-68-6
• Catalog Number: ACM5464686
• Category: Amines
• Molecular Weight: 195.15
• Molecular Formula: C₆H₁₃NO
• Hazard Statements: H302-H315-H318-H335
• RIDADR: NONH for all modes of transport
• Symbol: GHS05

Custom Q&A

What is the molecular formula of Diethyl carbamoylmethylphosphonate?

The molecular formula of Diethyl carbamoylmethylphosphonate is C6H14NO4P.

What are the synonyms of Diethyl carbamoylmethylphosphonate?

The synonyms of Diethyl carbamoylmethylphosphonate include Diethyl (2-amino-2-oxoethyl)phosphonate, 5464-68-6, 2-diethoxyphosphorylacetamide, Diethyl aminocarbonylmethylphosphonate.

What is the molecular weight of Diethyl carbamoylmethylphosphonate?

The molecular weight of Diethyl carbamoylmethylphosphonate is 195.15 g/mol.

What is the IUPAC name of Diethyl carbamoylmethylphosphonate?

The IUPAC name of Diethyl carbamoylmethylphosphonate is 2-diethoxyphosphorylacetamide.

What is the InChI of Diethyl carbamoylmethylphosphonate?

The InChI of Diethyl carbamoylmethylphosphonate is InChI=1S/C6H14NO4P/c1-3-10-12(9,11-4-2)5-6(7)8/h3-5H2,1-2H3,(H2,7,8).

What is the InChIKey of Diethyl carbamoylmethylphosphonate?

The InChIKey of Diethyl carbamoylmethylphosphonate is QPVCUQOSWAXEOQ-UHFFFAOYSA-N.

What is the canonical SMILES of Diethyl carbamoylmethylphosphonate?

The canonical SMILES of Diethyl carbamoylmethylphosphonate is CCOP(=O)(CC(=O)N)OCC.

What is the CAS number of Diethyl carbamoylmethylphosphonate?

The CAS number of Diethyl carbamoylmethylphosphonate is 5464-68-6.

Is Diethyl carbamoylmethylphosphonate a canonicalized compound?

Yes, Diethyl carbamoylmethylphosphonate is a canonicalized compound.

Synthetic Use

Upstream Synthesis Route 1

• 79-07-2
• 122-52-1

• 5464-68-6

Reference: [1] Journal of Organic Chemistry, 2009, vol. 74, # 23, p. 9140 - 9151
[2] Patent: WO2015/39173, 2015, A1, . Location in patent: Page/Page column 12; 13
[3] Journal of Organic Chemistry, 1959, vol. 24, p. 434
[4] Journal of Organic Chemistry, 1958, vol. 23, p. 1883,1885
[5] Pesticide Science, 1994, vol. 40, # 1, p. 57 - 62

Upstream Synthesis Route 2

• 867-13-0

• 5464-68-6

Reference: [1] Chemische Berichte, 1924, vol. 57, p. 1030[2] Chemische Berichte, 1926, vol. 59, p. 1120
[3] Roczniki Chemii, 1963, vol. 37, p. 949 - 954

Upstream Synthesis Route 3

• 683-57-8
• 122-52-1

• 5464-68-6

Reference: [1] Phosphorus, Sulfur and Silicon and Related Elements, 2000, vol. 160, p. 195 - 205

Upstream Synthesis Route 4

• 79-07-2
• 122-52-1

• 5464-68-6

Reference: [1]Journal of Organic Chemistry,2009,vol. 74,p. 9140 - 9151
[2]Patent: WO2015/39173,2015,A1 .Location in patent: Page/Page column 12; 13
[3]Journal of Organic Chemistry,1959,vol. 24,p. 434
[4]Pesticide Science,1994,vol. 40,p. 57 - 62

Downstream Synthesis Route 1

• 50-00-0
• 5464-68-6

• 37176-84-4

Reference: [1]Journal of general chemistry of the USSR,1972,vol. 42,p. 83 - 85
Zhurnal Obshchei Khimii,1972,vol. 42,p. 88 - 90

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