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1,1-dimethyl-4-methylenecyclohexane is an organic compound with the molecular formula C10H18. It is a cyclic alkane with a methylidene group (CH2) attached to the cyclohexane ring. The compound has two methyl groups (CH3) attached to the first carbon atom of the ring, and the methylene group is attached to the fourth carbon atom. This structure gives the compound a unique set of physical and chemical properties, making it useful in various chemical reactions and applications. It is a colorless liquid with a low boiling point and is insoluble in water but soluble in organic solvents. Due to its cyclic structure and the presence of methyl and methylene groups, 1,1-dimethyl-4-methylenecyclohexane exhibits a range of chemical reactivity, including the potential for addition, substitution, and elimination reactions.

6007-96-1

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6007-96-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6007-96-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,0 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6007-96:
(6*6)+(5*0)+(4*0)+(3*7)+(2*9)+(1*6)=81
81 % 10 = 1
So 6007-96-1 is a valid CAS Registry Number.

6007-96-1Downstream Products

6007-96-1Relevant academic research and scientific papers

Stereoselective Diboration of Spirocyclobutenes: A Platform for the Synthesis of Spirocycles with Orthogonal Exit Vectors

Nóvoa, Luis,Trulli, Laura,Parra, Alejandro,Tortosa, Mariola

, p. 11763 - 11768 (2021)

The diastereo- and enantioselective diboration of spirocyclobutenes provides a platform for the rapid preparation of a wide variety of chiral spirocyclic building blocks. The chemoselective functionalization of the carbon-boron bond in the products, including a stereospecific sp3-sp2 Suzuki–Miyaura cross-coupling reaction, provides a powerful tool to control the directionality and the nature of the exit vectors in the spirocyclic framework.

Expedient Access to 2,3-Dihydropyridines from Unsaturated Oximes by Rh(III)-Catalyzed C-H Activation

Romanov-Michailidis, Fedor,Sedillo, Kassandra F.,Neely, Jamie M.,Rovis, Tomislav

supporting information, p. 8892 - 8895 (2015/08/03)

α,β-Unsaturated oxime pivalates are proposed to undergo reversible C(sp2)-H insertion with cationic Rh(III) complexes to furnish five-membered metallacycles. In the presence of 1,1-disubstituted olefins, these species participate in irreversible migratory insertion to give, after reductive elimination, 2,3-dihydropyridine products in good yields. Catalytic hydrogenation can then be used to convert these molecules into piperidines, which are important structural components of numerous pharmaceuticals.

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