94982-29-3 Usage
Explanation
The compound is composed of two cations and one anion, with the cation containing four dimethylamino groups and two ethane bridges, and the anion containing two iodine atoms.
Explanation
The cationic part of the compound has a central ethylene (CH2CH2) bridge, with two nitrogen atoms connected to two methyl groups each.
Explanation
The anionic part of the compound consists of two iodine atoms, which balance the charge of the cation.
Explanation
The common name for this compound is not mentioned in the material provided.
Explanation
The compound is known for its high reactivity, making it useful in various organic synthesis reactions.
Explanation
Due to its reactivity, 1,1,2,2-tetrakis(dimethylamino)ethane-1,2-bis(ylium) diiodide has a wide range of potential applications in organic chemistry.
Explanation
The compound is commonly used as a source of diiodoalkenes, which can be used in various organic synthesis reactions, particularly in the formation of carbon-carbon double bonds.
Explanation
The compound's reactivity and versatility make it a valuable tool in the field of organic chemistry for various synthesis reactions and bond formations.
Structure
Cation with four dimethylamino groups and two ethane bridges
Anion
Two iodine atoms
Reactivity
Highly reactive
Versatility
Versatile compound
Applications
Source of diiodoalkenes, formation of carbon-carbon double bonds
Organic chemistry
Wide range of potential applications
Check Digit Verification of cas no
The CAS Registry Mumber 94982-29-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,9,8 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 94982-29:
(7*9)+(6*4)+(5*9)+(4*8)+(3*2)+(2*2)+(1*9)=183
183 % 10 = 3
So 94982-29-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H24N4.2HI/c1-11(2)9(12(3)4)10(13(5)6)14(7)8;;/h1-8H3;2*1H/q+2;;/p-2
94982-29-3Relevant articles and documents
Nickel-Catalyzed Reductive Dicarbofunctionalization of Alkenes
García-Domínguez, Andrés,Li, Zhaodong,Nevado, Cristina
supporting information, p. 6835 - 6838 (2017/06/01)
An intermolecular, three-component reductive dicarbofunctionalization of alkenes is presented here. The combination of Ni catalysis with TDAE as final reductant enables the direct formation of Csp3-Csp3 and Csp3-Csp2 bonds across a variety of π-systems using two different electrophiles that are sequentially activated with exquisite selectivity under mild reaction conditions.
