359786-37-1 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
It is a derivative of benzene, which is a basic structure consisting of a six-carbon ring with alternating single and double bonds.
Explanation
Aromatic amines are compounds that contain an amine group (-NH2) attached to an aromatic ring, in this case, the benzene ring.
Explanation
The compound is used in various industries, particularly in the production of dyes and pigments, including hair dyes, due to its chemical properties.
Explanation
The compound appears as a white to off-white solid when it is at room temperature.
Explanation
The compound has a high melting point, which means it requires a significant amount of heat to change from a solid to a liquid state.
Explanation
The compound is considered hazardous due to its potential health and environmental risks, and it should be handled with care and proper safety precautions.
Explanation
To minimize the risks associated with handling this hazardous compound, it is essential to follow safety guidelines, wear appropriate PPE, and take necessary precautions to prevent exposure or accidents.
Derivative of benzene
Yes
Classification
Aromatic amine
Applications
Production of dyes and pigments, hair dyes, and other chemical processes
Physical state at room temperature
White to off-white solid
Melting point
High
Hazardous nature
Yes
Safety precautions
Proper handling, use of personal protective equipment (PPE), and following safety guidelines
Check Digit Verification of cas no
The CAS Registry Mumber 359786-37-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,9,7,8 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 359786-37:
(8*3)+(7*5)+(6*9)+(5*7)+(4*8)+(3*6)+(2*3)+(1*7)=211
211 % 10 = 1
So 359786-37-1 is a valid CAS Registry Number.
359786-37-1Relevant academic research and scientific papers
Selective mono- and diamination of some polyhalogenbenzenes in anhydrous ammonia
Rodionov, Vladimir I.,Vaganova, Tamara A.,Malykhin, Evgenij V.
, p. 98 - 102 (2015/09/28)
Aminodefluorination of polyhalogenbenzenes (chloropentafluoro-, 1,3-dichlorotetrafluoro-, sym-trichlorotrifluoro-, 1,2,3,5-tetrafluoro- and 1,2,4,5-tetrafluoro-3-trifluoromethylbezenes) in anhydrous ammonia was investigated. The optimal conditions for sel
Catalytic and noncatalytic ammonolysis of chloropentafluorobenzene
Selivanova,Pokrovskii,Shteingarts
, p. 404 - 409 (2007/10/03)
Ammonolysis of chloropentafluorobenzene both in the presence and in the absence of copper(I) salt results mainly in replacement of the para-and ortho-fluorine atoms with respect to chlorine rather than replacement of the chlorine atom. Ammonolysis of 4-chloro-2,3,5,6-tetrafluoroaniline and 2-chloro-3,4,5,6-tetrafluoroaniline in the absence of copper(I) salt yields exclusively the corresponding fluorine substitution products, whereas in the presence of copper(I) salt the chlorine atom is replaced. Successive ammonolysis of chloropentafluorobenzene in the presence of copper catalyst along these two paths was put into the basis of a new method for preparation of 2,3,5,6-tetrafluoro-1,4-phenylenediamine. * This study was financially supported by the Russian Foundation for Basic Research (project no. 99-03-33111), by the Ministry of Science and Technology of the Russian Federation (project no 9.3.01), and by the Ministry of Education of the Russian Federation (project no. 015.05.01.13).
