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1-Methyltricyclo[2.2.1.02,?]heptane is a cyclic hydrocarbon compound with the molecular formula C?H??. It features a unique tricyclic structure, where three carbon rings are fused together in a specific arrangement. The compound has one methyl group attached to the first carbon atom of the central ring. This organic compound is known for its stability due to the rigid structure provided by the three fused rings. It is a colorless liquid at room temperature and is insoluble in water. 1-Methyltricyclo[2.2.1.02,?]heptane is primarily used as a chemical intermediate in the synthesis of various organic compounds and pharmaceuticals, taking advantage of its stable and complex structure.

4601-85-8

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4601-85-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4601-85-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,0 and 1 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4601-85:
(6*4)+(5*6)+(4*0)+(3*1)+(2*8)+(1*5)=78
78 % 10 = 8
So 4601-85-8 is a valid CAS Registry Number.

4601-85-8Downstream Products

4601-85-8Relevant academic research and scientific papers

Pyrolysis of Three Acetates of Methylbicycloheptan-2-ols and the Parent Alcohols

Vainiotalo, Pirjo,Pohjala, Esko,Maelkoenen, Pentti

, p. 1537 - 1540 (2007/10/02)

The acetates of exo-2-methyl-endo-bicycloheptan-2-ol, endo-2-methyl-exo-bicycloheptan-2-ol, and 1-methyl-exo-bicycloheptan-2-ol together the parent alcohols have been pyrolysed at several temperatures and the product distribution determined.The mechanism and direction of elimination in relation to structure are discussed qualitatively.The formation of the principal products is consistent with a concerted elimination involving a six-membered cyclic transition state.Wagner-Meerwein rearrangement occurs as a competing reaction in cases where the formation of a tertiary structure is possible at the expense of a secondary one.In the case studied a two-step reaction is considerably faster than direct pyrolysis of the secondary structure.

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