5859-45-0 Usage
Chemical structure
1-chloro-2-methyl-naphthalene is composed of a naphthalene ring with a chlorine atom and a methyl group attached to it.
Physical state
It is a colorless liquid.
Odor
1-chloro-2-methyl-naphthalene has a strong, sweet odor.
Solubility
It is insoluble in water but soluble in organic solvents.
Applications
a. Production of dyes and pigments.
b. Manufacturing of chemical intermediates.
c. Solvent for cellulose esters and ethers.
d. Manufacturing of photographic chemicals.
Environmental impact
1-chloro-2-methyl-naphthalene has been identified as a potential environmental hazard due to its persistence and toxicity.
Safety precautions
Caution should be exercised when handling and disposing of this chemical to minimize environmental and health risks.
Check Digit Verification of cas no
The CAS Registry Mumber 5859-45-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,5 and 9 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5859-45:
(6*5)+(5*8)+(4*5)+(3*9)+(2*4)+(1*5)=130
130 % 10 = 0
So 5859-45-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H9Cl/c1-8-6-7-9-4-2-3-5-10(9)11(8)12/h2-7H,1H3
5859-45-0Relevant articles and documents
Microwave assisted solid additive effects in simple dry chlorination reactions with n-chlorosuccinimide
Bucos, Madalina,Villalonga-Barber, Carolina,Micha-Screttas, Maria,Steele, Barry R.,Screttas, Constantinos G.,Heropoulos, Georgios A.
experimental part, p. 2061 - 2065 (2010/04/26)
Solid additives participate in the dry microwave assisted chlorination reaction of N-chlorosuccinimide with the xylenes affecting both yields and chemoselectivities. Total yields can be increased up to nine times for simple alkylaromatics and chemoselectivities can be altered according to the desired ring or α-side chlorination product by choosing the appropriate additive. We believe that in these reactions the solid additives play a very important role by increasing yields and affecting chemoselectivities, as well as behaving as microwave energy absorbers that consequently aid the transfer of heat to the active reagents.
