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79522

Sigma-Aldrich

tert-Butyl P,P-dimethylphosphonoacetate

≥97.0% (GC)

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Synonym(s):
tert-Butyl ((oxo)dimethoxyphosphino)acetate, tert-Butyl (dimethoxyphosphinyl)acetate, Dimethyl (tert-butoxycarbonyl)methylphosphonate
Linear Formula:
(CH3O)2P(O)CH2COOC(CH3)3
CAS Number:
Molecular Weight:
224.19
Beilstein:
4861886
MDL number:
UNSPSC Code:
12352108
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

≥97.0% (GC)

form

liquid

reaction suitability

reaction type: C-C Bond Formation

refractive index

n20/D 1.434

bp

86-87 °C/0.02 mmHg (lit.)

density

1.131 g/mL at 20 °C (lit.)

SMILES string

COP(=O)(CC(=O)OC(C)(C)C)OC

InChI

1S/C8H17O5P/c1-8(2,3)13-7(9)6-14(10,11-4)12-5/h6H2,1-5H3

InChI key

SAZYDWOWLRDDRQ-UHFFFAOYSA-N

Application

Reactant for:
  • Preparation of phosphonate terminated PPH dendrimers as anti-HIV-1 agents
  • Preparation of monodehydro diketopiperazines from ketoacyl amino acid amides via acid-catalyzed cyclization
  • Preparation of α,β-unsaturated esters for use in the guanidine-catalyzed oxa-Michael addition
  • Preparation of myxopyronin B and desmethyl myxopyronin B analogs, with antibacterial activity and inhibitory activity against bacterial RNA polymerase
  • Allylation and subsequent ring-closing metathesis in presence of Grubbs′ catalyst or intramolecular rhodium-catalyzed cyclopropanation reactions

Other Notes

Horner-Wittig reagent giving preferentially (E)-α,β-unsat. esters which are mildly saponified with acid. Synthesis of derivatives by reductive alkylation

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

WGK

WGK 3

Flash Point(F)

closed cup

Flash Point(C)

closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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G.W.J. Fleet et al.
Journal of the Chemical Society. Perkin Transactions 1, 905-905 (1984)
C. Kuroda et al.
The Journal of Organic Chemistry, 51, 956-956 (1986)
A novel synthesis of (+/-)-vermiculine.
Y Fukuyama et al.
Journal of the American Chemical Society, 99(2), 646-647 (1977-01-19)
W.J. Guilford et al.
Journal of the American Chemical Society, 109, 5013-5013 (1987)

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