64567-09-5 Usage
Derivative of naphthalene
Naphthalene is a hydrocarbon with two fused benzene rings, and 1-Iodo-3-nitronaphthalene is a modified version of naphthalene.
Contains a nitro group and an iodine atom
The presence of these two functional groups gives 1-Iodo-3-nitronaphthalene its unique chemical properties and reactivity.
Used as a reagent in organic synthesis
1-Iodo-3-nitronaphthalene is used to prepare various substituted naphthalene derivatives in chemical reactions.
Important intermediate in the production of pharmaceuticals, dyes, and agrochemicals
1-Iodo-3-nitronaphthalene is used as a starting material or building block in the synthesis of various commercial products.
Versatile reactivity and ability to undergo various chemical transformations
1-Iodo-3-nitronaphthalene can participate in a range of chemical reactions, making it a valuable compound in research and laboratory settings.
Hazardous and can cause skin and eye irritation
1-Iodo-3-nitronaphthalene is a dangerous chemical that can cause harm if not handled properly. It can irritate the skin and eyes upon contact.
Check Digit Verification of cas no
The CAS Registry Mumber 64567-09-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,5,6 and 7 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 64567-09:
(7*6)+(6*4)+(5*5)+(4*6)+(3*7)+(2*0)+(1*9)=145
145 % 10 = 5
So 64567-09-5 is a valid CAS Registry Number.
64567-09-5Relevant academic research and scientific papers
INDO- AND BENZINDOCYANINE DYES WITH FLUORINE-CONTAINING SUBSTITUENTS
Pazenok, S. V.,Kondratenko, N. V.,Popov, V. I.,Troitskaya, V. I.,Il'chenko, A. Ya.,et al.
, p. 1182 - 1187 (2007/10/02)
Syntheses are reported for 2,3,3-trimethyl-3H-indoles and 1,1,2-trimethyl-1H-benzindoles with fluorine-containing substituents (CF3, SCF3, and SO2CF3) at C-5 and for carbocyanine, merocyanine, and styryl dye derivatives of these indoles.The fluorine-containing substituents studied produce a bathochromic effect in the styryl dyes, hypsochromic effect in the merocyanine dyes, and, as a rule, a hypsochromic effect in the carbocyanine dyes.
