12321-46-9

Basic information

• Product Name: phenylnitromethane sodium salt
• Synonyms: phenylnitromethane sodium salt
• CAS NO: 12321-46-9
• Molecular Weight: 159.12
• Mol File: 12321-46-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: phenylnitromethane sodium salt(CAS DataBase Reference)
• NIST Chemistry Reference: phenylnitromethane sodium salt(12321-46-9)
• EPA Substance Registry System: phenylnitromethane sodium salt(12321-46-9)

Safety Data

• Hazardous Substances Data: 12321-46-9(Hazardous Substances Data)

Upstream product

• 622-42-4 1-nitro-1-phenylmethane 
• 140-29-4 phenylacetonitrile 

Downstream Products

• 622-42-4 1-nitro-1-phenylmethane 
• 100-52-7 benzaldehyde 
• 932-90-1 Benzaldoxime 
• 959-32-0 N-(benzoyloxy)benzamide 
• 588-59-0 stilbene 
• 30822-22-1 3-phenyl-5-(2,2,2-trifluoro-1-trifluoromethyl-ethylidene)-[1,4,2]dioxazole 
• 13440-25-0 (+/-)-1,2-dinitro-1,2-diphenylethane 
• 22020-72-0 triphenylizoxazole 
• 65-85-0 benzoic acid 
• 30822-26-5 O-Hexafluor-isobutyryl-benzhydroxamsaeure 
• 13286-95-8 meso-1,2-dinitro-1,2-diphenylethane 
• 15341-31-8 ((Z)-(1-nitroethene-1,2-diyl)dibenzene) 
• 1215-07-2 (E)-(1-nitroethene-1,2-diyl)dibenzene 
• 103-30-0 (E)-1,2-diphenyl-ethene 

Relevant articles and documents

Nonconventional versus conventional application of pseudo-first-order kinetics to fundamental organic reactions

Three new analysis procedures for pseudo-first-order kinetics are introduced and applied to eight different fundamental organic reactions. The reactions belong to the following classes: nitroalkane proton transfer, formal hydride ion transfers from NADH model compounds, and SN2 reactions of alkyl halides with ionic and neutral nucleophiles. The three methods consist of (1) half-life dependence of kapp, (2) sequential linear pseudo-first-order correlation, and (3) revised instantaneous rate constant analysis. Each of the three procedures is capable of distinguishing between one- and multistep mechanisms, and the combination of the three procedures provides a powerful strategy for differentiating between the two mechanistic possibilities. The data from the eight reactions chosen as examples clearly show how the procedures work in practice.