3750-83-2

Basic information

• Product Name: 4-Acetoxy-3-nitrohexane
• Synonyms: 4-Acetoxy-3-nitrohexane
• CAS NO: 3750-83-2
• Molecular Formula: C₈H₁₅NO₄
• Molecular Weight: 189.209
• Mol File: 3750-83-2.mol
• Article Data: 10

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-Acetoxy-3-nitrohexane(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Acetoxy-3-nitrohexane(3750-83-2)
• EPA Substance Registry System: 4-Acetoxy-3-nitrohexane(3750-83-2)

Safety Data

• Hazardous Substances Data: 3750-83-2(Hazardous Substances Data)

Upstream product

• 64-19-7 acetic acid 
• 108-03-2 1-Nitropropane 
• 108-24-7 acetic anhydride 
• 123-38-6 propionaldehyde 
• 5342-71-2 4-Nitrohexan-3-ol 
• 75-36-5 acetyl chloride 

Downstream Products

• 4812-22-0 2-ethyl-1-nitro-2-butene 
• 97336-41-9 ethyl 3,4-diethyl-1H-pyrrole-2-carboxylate 
• 147590-65-6 2-benzyl 3,4-diethyl-1H-pyrrole-2-carboxylate 
• 1006-26-4 3,4-diethylpyrrole-2-carbaldehyde 
• 30144-13-9 3,4-diethyl-1-methylpyrrole 
• 865855-40-9 2,5-bis((5-benzyloxycarbonyl-3-n-butyl-4-methyl-2-pyrrolyl)methyl)-3,4-diethyl-1H-pyrrole 
• 2683-82-1 2,3,7,8,12,13,17,18-octaethyl-porphyrin 
• 34874-30-1 3,4-diethyl-2-methyl-1H-pyrrole 
• 157873-93-3 3,4-diethyl-1H-pyrrole-2-carboxylic acid 
• 130274-66-7 3,4-diethyl-2,5-diformylpyrrole 
• 16200-52-5 3,4-diethyl-1H-pyrrole 
• 52921-22-9 3-ethyl-1H-pyrrole-2,4-dicarboxylic acid diethyl ester 

Relevant articles and documents

Synthesis of 2,2′-bipyrrole-5-carboxaldehydes and their application in the synthesis of B-ring functionalized prodiginines and tambjamines

Facile, versatile, and cost-effective synthetic routes for the preparation of a range of new 3-alkyl-, 4-alkyl-, 3,4-dialkyl-, and 3-halo-4-alkyl-2, 2′-bipyrrole-5-carboxaldehydes have been developed. These 2,2′-bipyrrole-5-carboxaldehydes offer interesting potential as building blocks for making bioactive natural and unnatural products, as demonstrated by the synthesis of B-ring functionalized prodiginines (PGs) and tambjamines.

Meso-unsubstituted iron corrole in hemoproteins: Remarkable differences in effects on peroxidase activities between myoglobin and horseradish peroxidase

(Figure Presented) Myoglobin (Mb) and horseradish peroxidase (HRP) were both reconstituted with a meso-unsubstituted iron corrole and their electronic configurations and peroxidase activities were investigated. The appearance of the 540 nm band upon incorporation of the iron corrole into apoMb indicates axial coordination by the proximal histidine imidazole in the Mb heme pocket. Based on 1H NMR measurements using the Evans method, the total magnetic susceptibility of the iron corrole reconstituted Mb was evaluated to be S = 3/2. In contrast, although a band does not appear in the vicinity of 540 nm during reconstitution of the iron corrole into the matrix of HRP, a spectrum similar to that of the iron corrole reconstituted Mb is observed upon the addition of dithionite. This observation suggests that the oxidation state of the corrole iron in the reconstituted HRP can be assigned as +4. The catalytic activities of both proteins toward guaiacol oxidation are quite different; the iron corrole reconstituted HRP decelerates H2O2-dependent oxidation of guaiacol, while the same reaction catalyzed by iron corrole reconstituted Mb has the opposite effect and accelerates the reaction. This finding can be attributed to the difference in the oxidation states of the corrole iron when these proteins are in the resting state.

Remarkable solvent effect in Barton-Zard pyrrole synthesis: application in an efficient one-step synthesis of pyrrole derivatives

A unique solvent effect encountered in the Barton-Zard pyrrole synthesis was exploited to develop an efficient synthesis of pyrrole-2-esters. The chemistry was extended to a one-pot synthesis of pyrrole-2,4-dicarboxylates.