345209-64-5 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 17 carbon (C) atoms, 14 hydrogen (H) atoms, 1 bromine (Br) atom, 1 nitrogen (N) atom, and 1 phosphorus (P) atom.
Explanation
The molecular weight is the sum of the atomic weights of all the atoms in the molecule. For 1H-Benzo[g]phosphindole, 3-bromo-2,3-dihydro-1-phenyl-, the molecular weight is approximately 366.2 grams per mole.
Explanation
The compound is classified as a heterocyclic compound because it contains a ring structure with atoms of different elements, specifically a phosphorous atom in addition to carbon, hydrogen, and nitrogen.
Explanation
The compound has a benzene ring (a six-membered ring with alternating double bonds), a phosphindole ring (a fused ring system containing a phosphorus atom), and a phenyl group (a benzene ring with a single bond to another carbon atom).
Explanation
The compound has a bromine atom (Br) attached to the third carbon atom in the phosphindole ring, indicating that it is a brominated derivative.
Explanation
The term "dihydro" indicates that two hydrogen atoms have been added to the molecule, specifically to the second and third carbon atoms in the phosphindole ring.
Explanation
Due to its unique structure and reactivity, 1H-Benzo[g]phosphindole, 3-bromo-2,3-dihydro-1-phenylis often used as a starting material or intermediate in the synthesis of more complex organic compounds and pharmaceuticals.
Explanation
The compound has been studied for its potential biological activities and pharmacological properties, which may lead to the development of new drugs and materials.
Explanation
As a complex organic molecule, 1H-Benzo[g]phosphindole, 3-bromo-2,3-dihydro-1-phenylis likely to be soluble in organic solvents such as dichloromethane, ethyl acetate, or acetone.
Explanation
The compound is generally stable under normal laboratory conditions, such as room temperature and ambient pressure, without undergoing significant decomposition or reaction.
Molecular Weight
366.2 g/mol
Structure
Heterocyclic compound with a phosphorous atom in the ring
Functional Groups
Benzene ring, phosphindole ring, and a phenyl group
Halogenation
3-bromo substitution
Hydrogenation
2,3-dihydro
Application
Building block in organic synthesis and pharmaceutical research
Biological Activities and Pharmacological Properties
Potential for drug development
Solubility
Soluble in organic solvents
Stability
Stable under normal conditions
Check Digit Verification of cas no
The CAS Registry Mumber 345209-64-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,5,2,0 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 345209-64:
(8*3)+(7*4)+(6*5)+(5*2)+(4*0)+(3*9)+(2*6)+(1*4)=135
135 % 10 = 5
So 345209-64-5 is a valid CAS Registry Number.
345209-64-5Relevant academic research and scientific papers
DEMONSTRATION OF C-PROTNATION OF PHOSPHOLES AND OF δ-DESHIELDING OF 31P USING MULTICYCLIC PHOSPHORUS COMPOUNDS
Quin, Louis D.,Mesch, Keith A.,Orton, William L.
, p. 161 - 178 (2007/10/02)
Cyclohexaphospholes and 4,5-dihydrobenzophosphindoles were synthesized by the dehydrobromination of the appropriate diene-phosphonous dihalide cycloadducts.The benzophosphindole system was constructed by NBS bromination of the 2,3-dihydro derivat
