41125-34-2 Usage
Nitro compound
A type of organic compound containing a nitro group (NO2) Indicates the presence of a nitro group in the structure.
Benzene ring
A six-carbon ring with alternating single and double bonds The core structure of the compound, which is a benzene ring.
Nitro group position
1 The nitro group (NO2) is attached at the first position on the benzene ring.
4-(4-phenylbutyl) group
A substituent consisting of a 4-phenylbutyl chain A specific group attached to the benzene ring, which influences the compound's properties and reactivity.
Organic synthesis
Frequently used in organic synthesis The compound is often employed as a building block or intermediate in the synthesis of other organic compounds.
Industrial applications
Production of pharmaceuticals, agrochemicals, and other organic compounds The compound has various uses in different industries, such as the production of pharmaceuticals and agrochemicals.
Importance in organic chemistry
A versatile compound with a range of potential uses The compound is significant in the field of organic chemistry due to its adaptability and wide range of applications.
Check Digit Verification of cas no
The CAS Registry Mumber 41125-34-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,1,2 and 5 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 41125-34:
(7*4)+(6*1)+(5*1)+(4*2)+(3*5)+(2*3)+(1*4)=72
72 % 10 = 2
So 41125-34-2 is a valid CAS Registry Number.
41125-34-2Relevant academic research and scientific papers
Visible Light-Driven, Room Temperature Heck-Type Reaction of Alkyl Halides with Styrene Derivatives Catalyzed by B12 Complex
Chen, Li,Hisaeda, Yoshio,Shimakoshi, Hisashi
, p. 2877 - 2884 (2019/04/03)
A visible light driven Heck-type coupling reaction of alkyl halides with styrene and its derivatives catalyzed by the cobalamin derivative (B12) with the [Ru(bpy)3]Cl2 photosensitizer at room temperature is reported. The catalytic efficiencies of the B12 catalyst were compared to that of other cobalt complexes such as cobaloxime. Various control experiments supported a radical-based mechanism similar to those for typical B12 model reactions. A unique coupling reaction combined with 1,2-migration of the functional group is also reported. Mild reaction conditions using an environmentally benign cobalt catalyst derived from the natural B12 provided a practical protocol for the synthetic organic chemistry of the B12 catalyzed reaction system. (Figure presented.).
Macrocycle Formation via Arylnitrenium Ions: Possible Intramolecular Recognition
Abramovitch, Rudolph A.,Shi, Qing
, p. 2147 - 2152 (2007/10/02)
MMX calculations on 1-(4-nitrophenyl)-9-phenylnonane indicate that it has a global minimum energy conformation in which the aryl rings are within easy bonding distance, which is confirmed by 2D NOESY, ultraviolet and fluorescence spectroscopy; the corresp
