90485-88-4 Usage
Nitroalkane compound
A class of organic compounds that contains a nitro group (NO2) attached to an alkane chain, indicating the presence of oxygen and nitrogen in the molecule.
Straight-chain pentane structure
The carbon atoms in the compound are arranged in a linear or straight configuration, which is typical for alkanes.
Nitro group at the 1-position
A nitro group (NO2) is attached to the first carbon atom in the pentane chain, which influences the compound's reactivity and properties.
Nitromethyl group at the 2-position
A nitromethyl group (CH2NO2) is attached to the second carbon atom in the pentane chain, further affecting the compound's reactivity and properties.
Intermediate in synthesis
1-nitro-2-(nitromethyl)pentane is primarily used as an intermediate in the synthesis of various organic compounds, making it a valuable building block in organic chemistry.
Research applications
The compound is used in research laboratories for chemical reactions and studies, providing valuable insights into the behavior of nitroalkanes and related compounds.
Explosive properties
1-nitro-2-(nitromethyl)pentane is known for its explosive properties, which can pose a risk in laboratory settings if not handled properly.
Caution required
Due to its explosive nature, special care and precautions must be taken when handling, storing, and working with 1-nitro-2-(nitromethyl)pentane in laboratory environments.
Check Digit Verification of cas no
The CAS Registry Mumber 90485-88-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,4,8 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 90485-88:
(7*9)+(6*0)+(5*4)+(4*8)+(3*5)+(2*8)+(1*8)=154
154 % 10 = 4
So 90485-88-4 is a valid CAS Registry Number.
90485-88-4Relevant articles and documents
Michael addition at neutral pH: A facile synthesis of 1,3-dinitroalkanes
Bora, Porag,Bora, Pranjal P.,Wahlang, Barisha,Bez, Ghanashyam
, p. 1261 - 1266 (2017/11/27)
Base-catalyzed Michael addition of nitroalkane to conjugated nitroalkene suffers serious practical difficulties due to the formation of oligomeric byproduct. Given its importance for synthesis of pharmacologically relevant organic compounds, a scalable synthesis of 1,3-dinitroalkane is developed by addition of nitroalkane to nitroalkene in aqueous phosphate buffer at pH 7.0 with no added traditional base catalyst.
