26251-08-1

Basic information

• Product Name: 2-nitro-1-phenylpropan-1-ol
• CAS NO: 26251-08-1
• Molecular Weight: 181.191
• Mol File: 26251-08-1.mol
• Article Data: 46

Chemical Properties

• CAS DataBase Reference: 2-nitro-1-phenylpropan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-nitro-1-phenylpropan-1-ol(26251-08-1)
• EPA Substance Registry System: 2-nitro-1-phenylpropan-1-ol(26251-08-1)

Safety Data

• Hazardous Substances Data: 26251-08-1(Hazardous Substances Data)

Upstream product

• 75-52-5 nitromethane 
• 100-52-7 benzaldehyde 
• 79-24-3 Nitroethane 
• 100-51-6 benzyl alcohol 
• 14897-67-7 2-nitropropiophenone 
• 705-60-2 (2-nitroprop-1-enyl)benzene 

Downstream Products

• 68398-02-7 β-o-vanillylamino-α-phenyl-propyl alcohol 
• 1493-93-2 1-<4-Fluorphenyl>-2-nitro-1-phenyl-propan 
• 16251-45-9 4,5-trans-4-Methyl-5-phenyl-1,3-oxazolidin-2-one 
• 94768-24-8 erythro-N-(2-nitro-1-phenylpropyl)acetamide 
• 16251-45-9 (4S,5R)-4-methyl-5-phenyl-oxazolidin-2-one 
• 130564-44-2 N-(2-nitro-1-phenylpropyl)benzamide 
• 1434076-44-4 (1R,2S)-1-phenyl-N¹,N²-bis((S)-1-phenylethyl)propane-1,2-diamine 

Relevant articles and documents

Copper complexes of 1,4-diazabutadiene ligands: Tuning of metal oxidation state and, application in catalytic C-C and C-N bond formation

Reaction of 1,4-diazabutadiene (p-RC6H4N = C(H)(H)C = NC6H4R-p; R = OCH3, CH3, H and Cl; abbreviated as L-R) with CuCl2·2H2O in methanol at ambient temperature (25 °C) affords a group of doubly chloro-bridged dicopper complexes of type [{CuI(L-R)Cl}2], designated as 1-R. Similar reaction carried out in acetonitrile furnishes a family of doubly chloro-bridged dicopper complexes of type [{CuII(L-R)Cl2}2], designated as 2-R. Molecular structures of 1-OCH3 and 2-OCH3 have been determined by X-ray crystallography. While copper(I) is having a nearly tetrahedral N2Cl2 coordination sphere in 1-OCH3, the N2Cl3 coordination sphere around copper(II) is distorted square pyramidal in nature in 2-OCH3. Isolated 2-R complexes, on dissolution in methanol, are found to undergo facile reduction of the metal center to generate the corresponding 1-R complexes. The 1-R and 2-R complexes show intense absorptions in the visible and ultraviolet regions. Cyclic voltammetry on the 1-R and 2-R complexes shows both metal-centered and ligand centered redox responses. The 1-R complexes are found to efficiently catalyze C-N cross-coupling reactions between arylboronic acids and aryl amines; while the 2-R complexes display notable catalytic efficiency for nitroaldol reactions.

Ultrasound-assisted synthesis of two new fluorinated metal-organic frameworks (F-MOFs) with the high surface area to improve the catalytic activity

Micro- and nano-structures of two zinc(II) based fluorinated metal-organic frameworks (F-MOFs) [Zn2(hfipbb)2(4-bpdh)].(DMF)0.5 (TMU-55) and [Zn2(hfipbb)2(4-bpdb)].(DMF)2 (HTMU-55) with micr

A nitroaryloxy aromatic preparation method (by machine translation)

The invention discloses a nitroaryloxy aromatic preparation method, comprises the following steps: a, will R1 CHO, R2 CH2 NO2 , Catalyst and a polar organic solvent evenly, 0 °C -40 °C stirring for 6 hours -48 h