46000-10-6 Usage
Chemical composition
1-NAPHTHYLZINC IODIDE is composed of a zinc atom bonded to a 1-naphthyl group and an iodide ion.
Use as a reagent
It is commonly used as a reagent in organic synthesis.
Specific field of use
1-NAPHTHYLZINC IODIDE is particularly used in the field of organometallic chemistry.
Role in cross-coupling reactions
It is known for its role in cross-coupling reactions.
Use as a catalyst
1-NAPHTHYLZINC IODIDE acts as a catalyst in various chemical transformations.
Potential applications
It has been studied for its potential applications in the development of new materials and pharmaceuticals.
Unique properties
1-NAPHTHYLZINC IODIDE has unique properties that make it a valuable tool for researchers and chemists working to develop new chemical processes and compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 46000-10-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,6,0,0 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 46000-10:
(7*4)+(6*6)+(5*0)+(4*0)+(3*0)+(2*1)+(1*0)=66
66 % 10 = 6
So 46000-10-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H7.HI.Zn/c1-2-6-10-8-4-3-7-9(10)5-1;;/h1-7H;1H;/q-1;;+2/p-1/rC10H7.IZn/c1-2-6-10-8-4-3-7-9(10)5-1;1-2/h1-7H;/q-1;+1
46000-10-6Relevant articles and documents
Synthesis of polybenzoquinazolines via an intramolecular dehydration of photocyclization
Wei, Wei,Li, Chenchen,Wang, Tao,Liu, Dian,Zhang, Zunting
, p. 5037 - 5046 (2016/07/25)
Benzo[h]-naphth[1,2-f]quinazolines and benzo[h]-phenanthren[9,10-f]quinazoines were synthesized from intermediates 4-(2-hydroxyphenyl)-5-(naphthalen-1-yl)pyrimidines and 4-(2-hydroxyphenyl)-5-(phenanthren-1-yl) pyrimidines by the intramolecular dehydration of photocyclization. The intermediates were obtained by the condensation of 3-arylchromone with formamidine, acetamidine or guanidine refluxing in ethanol, respectively. Irradiation of the corresponding intermediates by a high-pressure mercury lamp in 19:1 (v/v) [Formula presented]2O or 18:1:1 (v/v) [Formula presented]2O-Dioxane lead to target products. This photocyclization showed advantages including catalyst-free and mild reaction condition. Moreover, water was the only by-product of this reaction. The crystal structure of 2-amino-12-methoxy-benzo[h]-naphth[1,2-f]quinazoline was determined and the fluorescence properties of these polybenzoquinazolines were also investigated.
