950-94-7 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
The compound consists of two benzene rings connected at the 1st position, with a nitro group (-NO2) attached to one of the rings and a chlorine atom (-Cl) attached to the other.
Explanation
The compound is used in various industries due to its chemical properties, which make it suitable for the production of different products.
Explanation
Due to its chemical nature, 2-chloro-2'-nitro-1,1'-biphenyl is classified as a hazardous chemical, which means it can pose risks to human health and the environment if not handled properly.
Explanation
Given its hazardous nature, it is essential to follow safety protocols and guidelines when working with 1,1'-Biphenyl, 2-chloro-2'-nitro- to minimize the risk of exposure and potential harm.
Explanation
The compound belongs to the class of aromatic compounds, which are characterized by the presence of a benzene ring in their structure.
Explanation
The presence of nitro and chloro functional groups in the molecule contributes to its chemical reactivity and potential applications in various industries.
Structure
Nitro-substituted biphenyl derivative with a chlorine atom
Applications
Dyes, pigments, pharmaceuticals, and synthesis of other organic compounds
Hazardous chemical
Potential health and environmental risks
Handling precautions
Should be handled with caution
Chemical class
Aromatic compound
Functional groups
Nitro (-NO2) and chloro (-Cl) groups
Check Digit Verification of cas no
The CAS Registry Mumber 950-94-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,5 and 0 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 950-94:
(5*9)+(4*5)+(3*0)+(2*9)+(1*4)=87
87 % 10 = 7
So 950-94-7 is a valid CAS Registry Number.
950-94-7Relevant academic research and scientific papers
Gonzalez, Raquel Rodriguez,Liguori, Lucia,Carrillo, Alberto Martinez,Bjorsvik, Hans-Rene
, p. 9591 - 9594 (2005)
Mechanistic investigations and protocols for the synthesis of 2-nitrobiphenyls and 2,2′-dinitrobiphenyls are disclosed. It is revealed that obstacles appear during the transmetalation step when the phenylboronic acid is substituted with a nitro group in the 2-position, whereas when substituted in the 3- or 4-positions, the reaction follows similar patterns as found in the electrophilic substitution of nitrobenzenes, an observation that may be attributed to the elimination step of the catalytic cycle.
