40422-46-6 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
The IUPAC name is a standardized nomenclature system used to name chemical compounds.
Explanation
It has two interconnected rings, making it a bicyclic compound.
Explanation
The compound contains a six-membered ring, which is a common structural feature in many organic compounds.
Explanation
The compound is a salt formed by the reaction of 1,5-Diazocine with hydrobromic acid (HBr), resulting in the dihydrobromide salt.
Explanation
It is commonly used as a reagent in the synthesis of various organic compounds.
Explanation
The compound is used in pharmaceutical research for the development of new drugs and therapies.
Explanation
It has been investigated for its potential use in the treatment of various medical conditions, including cancer and neurological disorders.
Explanation
Its properties and uses make it an important compound in the field of medicinal chemistry and drug development.
Explanation
The compound is soluble in water and certain organic solvents, which is important for its use in chemical reactions and pharmaceutical applications.
Bicyclic Organic Compound
Yes
Six-membered Ring
Yes
Dihydrobromide Salt
Yes
Reagent in Organic Synthesis
Yes
Pharmaceutical Research
Yes
Potential Medical Applications
Cancer and neurological disorders
Importance in Medicinal Chemistry
High
Solubility
Soluble in water and some organic solvents
Check Digit Verification of cas no
The CAS Registry Mumber 40422-46-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,4,2 and 2 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 40422-46:
(7*4)+(6*0)+(5*4)+(4*2)+(3*2)+(2*4)+(1*6)=76
76 % 10 = 6
So 40422-46-6 is a valid CAS Registry Number.
40422-46-6Relevant articles and documents
DEPROTONATION OF HYDRAZINIUM DICATIONS IN THE DIAZONIAPROPELLANE SERIES TO FORM BRIDGEHEAD IMINIUM IONS; EXTERNAL AND INTRAMOLECULAR TRAPPING
Alder, Roger W.,Sessions, Richard B.,Gmuender, John O.,Grob, Cyril A.
, p. 411 - 418 (2007/10/02)
The reactions of hexa-alkylhydrazinium dications with bases and nucleophiles are described. 1,5-Diazonia-tricyclodecane (1) is hydrolysed rapidly by SN2 attack on the four-membered ring with ring opening (C-N+ cleavage).In all other cases deprotonation at α-C with concomitant N+-N+ cleavage (E2 reaction) is the only primary process.The cis-1,6-dimethyl-1,6-diazoniabicyclodecane ion (6), is exclusively deprotonated at a methyl group (Hofmann orientation). 1,5-Diazoniatricycloundecane (2), 1,6-diazoniatricyclododecane (3), 1,6-diazoniatricyclotridecane (4), and 1,6-diazoniatricyclotetradecane (5) ions generate bridgehead iminium ions, which may be trapped intramolecularly by the transannular amino group or externally by added nucleophiles.Reaction with cyanide ion gives detailed information on the regio- and stereo-chemistry of the trapping sequence.Although intramolecular/external trapping is truly competitive, the products of these reactions (α-amino-ammonium ions and α-aminonitriles) may be interconverted under different reaction conditions.The solvolysis of 1-(3-phenoxypropyl)-1,5-diazabicyclooctanium bromide in aqueous 48percent HBr is 103 faster than that of 3-phenoxypropyltrimethylammonium bromide, and the products are consistent with the intermediacy of the dication (2).These observations provide an explanation for the formation of 1,5-diazacyclo-octane in the reaction of 1,3-dibromopropane with hydrazine.
