89894-77-9 Usage
Haloalkane
A halogenated cyclohexane
1-iodo-3-methylcyclohexane is a type of haloalkane, which means it is an organic compound containing a halogen atom bonded to an alkane (in this case, cyclohexane).
Methyl group
CH3
A methyl group (CH3) is a small alkyl group derived from methane, consisting of one carbon atom bonded to three hydrogen atoms.
Iodine atom
Attached to the cyclohexane ring
An iodine atom is a non-metal element from the halogen group, which is attached to the cyclohexane ring in 1-iodo-3-methylcyclohexane.
Organic synthesis
Reactant in chemical reactions
1-iodo-3-methylcyclohexane is commonly used as a reactant in various organic synthesis processes, such as nucleophilic substitution and elimination reactions.
Preparation of other organic compounds
Research and laboratory experiments
1-iodo-3-methylcyclohexane can be used in the preparation of other organic compounds and is also utilized in research and laboratory experiments.
Potentially hazardous chemical
Safety precautions and procedures
1-iodo-3-methylcyclohexane is considered a potentially hazardous chemical, and it should be handled with care, following proper safety precautions and procedures to minimize risks.
Check Digit Verification of cas no
The CAS Registry Mumber 89894-77-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,8,9 and 4 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 89894-77:
(7*8)+(6*9)+(5*8)+(4*9)+(3*4)+(2*7)+(1*7)=219
219 % 10 = 9
So 89894-77-9 is a valid CAS Registry Number.
89894-77-9Relevant academic research and scientific papers
Cobalt-Catalyzed Cross-Coupling of Functionalized Alkylzinc Reagents with (Hetero)Aryl Halides
Grokenberger, Lucie,Hammann, Jeffrey M.,Karaghiosoff, Konstantin,Knochel, Paul,Lutter, Ferdinand H.,Spie?, Philipp
supporting information, p. 5546 - 5550 (2020/02/26)
A combination of 10 % CoCl2 and 20 % 2,2′-bipyridine ligands enables cross-coupling of functionalized primary and secondary alkylzinc reagents with various (hetero)aryl halides. Couplings with 1,3- and 1,4-substituted cycloalkylzinc reagents proceeded diastereoselectively leading to functionalized heterocycles with high diastereoselectivities of up to 98:2. Furthermore, alkynyl bromides react with primary and secondary alkylzinc reagents providing the alkylated alkynes.
