6329-58-4 Usage
Nitroalkane derivative
A class of compounds that have a nitro group (-NO2) attached to an alkane carbon chain, contributing to the compound's reactivity and explosive properties.
Phosphoryl group
A functional group (P=O) present in the compound, which is a phosphorus atom double-bonded to an oxygen atom, providing stability and reactivity to the molecule.
Diethoxy functional group
A functional group (-O-CH2-CH3)2 present in the compound, consisting of two ethoxy groups attached to a phosphorus atom, contributing to the compound's unique chemical properties.
Precursor in organophosphorus synthesis
1-diethoxyphosphoryl-1-nitro-propane is commonly used as a starting material in the synthesis of various organophosphorus compounds, which have a wide range of applications in agriculture, pharmaceuticals, and materials science.
Production of pesticides and insecticides
The compound is used in the formulation of pesticides and insecticides, helping to control pests and insects in agricultural and domestic settings.
Pharmaceutical preparation
1-diethoxyphosphoryl-1-nitro-propane is also used as an intermediate in the synthesis of pharmaceuticals, contributing to the development of new drugs and therapies.
Colorless to pale yellow liquid
The compound's physical appearance, which can range from colorless to pale yellow, with a characteristic odor.
Check Digit Verification of cas no
The CAS Registry Mumber 6329-58-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,2 and 9 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6329-58:
(6*6)+(5*3)+(4*2)+(3*9)+(2*5)+(1*8)=104
104 % 10 = 4
So 6329-58-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H16NO5P/c1-4-7(8(9)10)14(11,12-5-2)13-6-3/h7H,4-6H2,1-3H3
6329-58-4Relevant academic research and scientific papers
Enantioselective synthesis of quaternary α-aminophosphonates via conjugate addition of α-nitrophosphonates to enones
Bera, Kalisankar,Namboothiri, Irishi N. N.
supporting information; experimental part, p. 980 - 983 (2012/04/04)
Enantioselective Michael addition of α-nitrophosphonates to enones for the synthesis of α-aminophosphonates is reported for the first time. The reaction proceeds in good to high yields and moderate to high selectivity in the presence of a new quinine thio
A New Method for the Preparation of Conjugated Nitro Olefins
Fujii, Masayuki
, p. 933 - 934 (2007/10/02)
Condensation of 1-nitroalkanephosphonates with carbonyl compounds affords a new and facile method for the preparation of conjugated nitro olefins.
One-step Synthesis of Stabilized Phosphonates
Kandil, Ali A.,Porter, Terence M.,Slessor, Keith N.
, p. 411 - 413 (2007/10/02)
Phosphonates possessing α-electron withdrawing functionalities can be readily prepared by treatment of nitriles, nitroalkanes, and esters with 2 molar equivalents of base followed by phosphonylation with diethyl chlorophosphate.
