CAS 1606-30-0

2-methyl-1-nitroprop-1-ene

Description:

2-Methyl-1-nitroprop-1-ene, with the CAS number 1606-30-0, is an organic compound characterized by its structure, which includes a nitro group (-NO2) attached to a propene backbone. This compound features a double bond between the first and second carbon atoms, contributing to its reactivity and potential applications in organic synthesis. The presence of the methyl group at the second carbon enhances its stability and influences its chemical behavior. Typically, nitroalkenes like 2-methyl-1-nitroprop-1-ene are known for their electrophilic properties, making them useful intermediates in various chemical reactions, including nucleophilic additions and cycloadditions. The compound is likely to be a colorless to pale yellow liquid, exhibiting moderate volatility and solubility in organic solvents. Safety considerations should be taken into account, as nitro compounds can be hazardous and may require careful handling and storage. Overall, 2-methyl-1-nitroprop-1-ene is a valuable compound in synthetic organic chemistry, with potential applications in the development of pharmaceuticals and agrochemicals.

Formula: C₄H₇NO₂

InChI: InChI=1/C4H7NO2/c1-4(2)3-5(6)7/h3H,1-2H3

SMILES: CC(=CN(=O)=O)C

Synonyms:

• 1-Propene, 2-methyl-1-nitro-
• 2-Methyl-1-nitro-1-propene

2-Methyl-1-nitroprop-1-ene

CAS: 1606-30-0

Formula: C₄H₇NO₂

Molecular weight: 101.1039

Ref: IN-DA00HYLQ

2-Methyl-1-nitroprop-1-ene

CAS: 1606-30-0

2-Methyl-1-nitroprop-1-ene

Formula: C₄H₇NO₂

Purity: ≥95%

Color and Shape: Solid

Molecular weight: 101.10g/mol

Ref: 54-OR310840

2-Methyl-1-nitroprop-1-ene

CAS: 1606-30-0

Purity: 98%

Molecular weight: 101.1050033569336

Ref: 10-F770444

2-Methyl-1-nitroprop-1-ene

CAS: 1606-30-0

2-Methyl-1-nitroprop-1-ene is a labile molecule that can be readily synthesized from 2-methyl propanal and nitrous acid. The postulated reaction mechanism for the formation of 2-methyl-1-nitroprop-1-ene begins with the nucleophilic attack of the azide anion on the carbonyl group of 2 methyl propanal, forming a tetrahedral intermediate. This intermediate undergoes a stepwise reaction to form 2 methyl 1 nitropropane. Nitro groups have been observed in both the product and starting material, which could indicate a transfer mechanism.

Formula: C₄H₇NO₂

Purity: Min. 95%

Color and Shape: Clear Liquid

Molecular weight: 101.1 g/mol

Ref: 3D-FM39234