ChemicalBook--->CAS DataBase List--->62327-21-3

62327-21-3

62327-21-3 Structure

62327-21-3 Structure
IdentificationBack Directory
[Name]

tert-Butyl O,O-dimethylphosphonoacetate
[CAS]

62327-21-3
[Synonyms]

MRIO-005
P,P-dimethyL
Dimethyl (Boc-methyl)phosphonate
tert-Butyl 2-(dimethoxyphosphoryl)
Tert-butyl dimethylphosphonoactate
tert-Butyl dimethylphosphonoacetate
Tert-butyl dimethyl phosphonylacetate
tert-Butyl (dimethoxyphosphinyl)acetate
TERT-BUTYL P,P-DIMETHYLPHOSPHONOACETATE
tert-Butyl O,O-dimethylphosphonoacetate
tert-Butyl 2-(diMethoxyphosphoryl)acetate
tert-Butyl ((oxo)dimethoxyphosphino)acetate
Dimethylphosphonoacetic Acid tert-Butyl Ester
DIMETHYL TERT-BUTOXYCARBONYL-METHYLPHOSPHONATE
tert-Butyl P,P-diMethylphosphonoacetate, >= 97.0 % GC
Acetic acid, 2-(dimethoxyphosphinyl)-, 1,1-dimethylethyl ester
[Molecular Formula]

C8H17O5P
[MDL Number]

MFCD00042939
[MOL File]

62327-21-3.mol
[Molecular Weight]

224.19
Chemical PropertiesBack Directory
[Boiling point ]

86-87 °C0.02 mm Hg(lit.)
[density ]

1.131 g/mL at 20 °C(lit.)
[refractive index ]

n20/D 1.434
[Fp ]

110 ºC
[storage temp. ]

Inert atmosphere,2-8°C
[form ]

clear liquid
[color ]

Colorless to Almost colorless
[BRN ]

4861886
[InChI]

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

SAZYDWOWLRDDRQ-UHFFFAOYSA-N
[SMILES]

C(OC(C)(C)C)(=O)CP(OC)(OC)=O
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P302+P352-P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26
[WGK Germany ]

3
[F ]

9-23
[HS Code ]

2931.39.0030
[Storage Class]

10 - Combustible liquids
[Hazard Classifications]

Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Hazard InformationBack Directory
[Uses]

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
[reaction suitability]

reaction type: C-C Bond Formation
Spectrum DetailBack Directory
[Spectrum Detail]

tert-Butyl 2-(dimethoxyphosphoryl)acetate(62327-21-3)1HNMR
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