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1-Methyltricyclo[2.2.1.0~2,6~]hept-3-yl formate is a complex organic compound with the molecular formula C10H15O2. It is a derivative of tricyclo[2.2.1.0~2,6~]heptane, featuring a methyl group attached to the first carbon atom and a formate group (-OOCCH3) at the third carbon position. 1-methyltricyclo[2.2.1.0~2,6~]hept-3-yl formate is characterized by its unique tricyclic structure, which consists of three fused rings with varying sizes. The compound is of interest in organic chemistry and may have potential applications in the synthesis of pharmaceuticals or other specialty chemicals due to its specific structural features. However, it is important to note that the compound's properties, reactivity, and applications would need to be further explored and characterized through experimental studies.

3197-60-2

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3197-60-2 Usage

Classification

Chemical compound
Fragrant ester

Common sources

Essential oils (e.g., pine and fir oils)

Odor

Pleasant, fresh, and woody

Usage

Fragrance ingredient in cosmetic and household products

Medicinal properties

Anti-inflammatory and antimicrobial effects

Potential applications

Insect repellent due to natural origin and pest-deterring abilities

Check Digit Verification of cas no

The CAS Registry Mumber 3197-60-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,9 and 7 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3197-60:
(6*3)+(5*1)+(4*9)+(3*7)+(2*6)+(1*0)=92
92 % 10 = 2
So 3197-60-2 is a valid CAS Registry Number.

3197-60-2Downstream Products

3197-60-2Relevant academic research and scientific papers

ADDITION OF ACETIC ACID TO 5-METHYLENE- AND 5-METHYL-6-METHYLENEBICYCLOHEPT-2-ENE

Bobyleva, A. A.,Dubitskaya, N. F.,Pekhk, T. I.,Belikova, N. A.

, p. 921 - 927 (2007/10/02)

The reaction of acetic acid with 5-methylene- and 5-methyl-6-methylenebicyclohept-2-ene takes place through protonation of the semicyclic double bond with the intermediate formation of a homoallylic ion.When the reaction was realized under kinetically controlled conditions, the tertiary acetates of endo-5-methyl- and endo,endo-5,6-dimethylbicyclohept-2-en-exo-5-ol were obtained; the final products were only the esters of 1-methyl- and 1,7-dimethyltricyclo2,6>heptan-3-ol.The rate of the reaction of 5-methyl-6-methylenebicyclohept-2-ene with acetic acid was determined.The reactions are proposed as methods for the production of esters and also of alcohols, ketones, and hydrocarbons with the tricyclo2,6> heptane structure.

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