6625-54-3 Usage
Uses
Used in Organic Synthesis:
1-(chloromethyl)-5-nitro-naphthalene is used as a building block for the preparation of various pharmacologically active molecules and other organic compounds. Its chloromethyl group makes it reactive towards nucleophiles, allowing it to participate in a variety of chemical reactions such as substitution and addition reactions. The nitro group also makes it an electron-withdrawing group, affecting the reactivity and physical properties of the compound.
Check Digit Verification of cas no
The CAS Registry Mumber 6625-54-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,2 and 5 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6625-54:
(6*6)+(5*6)+(4*2)+(3*5)+(2*5)+(1*4)=103
103 % 10 = 3
So 6625-54-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H8ClNO2/c12-7-8-3-1-5-10-9(8)4-2-6-11(10)13(14)15/h1-6H,7H2
6625-54-3Relevant academic research and scientific papers
INTRAMOLECULAR ELECTRON TRANSFER AND DEHALOGENATION OF NITROAROMATIC ANION RADICALS.
Bays,Blumer,Baral-Tosh,Behar,Neta
, p. 320 - 324 (2007/10/02)
A series of nitroaromatic compounds, containing Cl, Br or tosyl groups at various positions, were synthesized and studied by pulse radiolysis in aqueous alcohol solutions. One-electron reduction of the compounds produces the anion radicals which then undergo an intramolecular electron transfer and eliminate X** minus (Cl** minus , Br** minus , or TsO** minus ). The rates of X** minus elimination vary over six orders of magnitude and are affected by the C-X bond dissociation energies, the size and nature of the group bridging the X with the pi system, and the relative positions of these groups. Intramolecular electron transfer through space is also demonstrated. Refs.
