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Bicyclo[2.2.1]heptan-2-one, 3,3-dimethyl-, (1S)-, also known as cis-3,3-dimethylbicyclo[2.2.1]heptan-2-one, is an organic compound with the molecular formula C9H14O. It is a cyclic ketone with a bicyclic structure, featuring two methyl groups at the 3-position and a chiral center at the 1-position, resulting in the (1S)-configuration. Bicyclo[2.2.1]heptan-2-one, 3,3-dimethyl-, (1S)- is characterized by its unique stereochemistry and is used in the synthesis of various organic compounds, particularly in the pharmaceutical and fragrance industries. It is known for its ability to contribute to the formation of complex molecular structures and is often employed as an intermediate in the production of more complex molecules.

6069-71-2

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6069-71-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6069-71-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,6 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6069-71:
(6*6)+(5*0)+(4*6)+(3*9)+(2*7)+(1*1)=102
102 % 10 = 2
So 6069-71-2 is a valid CAS Registry Number.

6069-71-2Upstream product

6069-71-2Relevant academic research and scientific papers

Thermal degradation of terpenes: Camphene, Δ3-carene, limonene, and α-terpinene

Mcgraw, Gerald W.,Hemingway, Richard W.,Ingram Jr., Leonard L.,Canady, Catherine S.,Mcgraw, William B.

, p. 4029 - 4033 (2007/10/03)

Emissions from wood dryers have been of some concern for a number of years, and recent policy changes by the Environmental Protection Agency have placed emphasis upon the gaseous emissions that lead to the formation of particulate matter as small as 2.5 μm diameter. In this qualitative study, camphene, Δ3-carene, limonene, and α-terpinene were thermally degraded in the presence of air to determine the number and kind of oxidative degradation products that might be expected under drying conditions used in processing wood products. Various chromatographic methods were used to isolate the products for proof of structure by NMR and/or GC-MS. The degradation products resulted from dehydrogenations, epoxidations, double bond cleavages, allylic oxidations, and rearrangements. A number of compounds not previously associated with the thermal degradation of these terpenes were identified. Emissions from wood dryers have been of some concern for a number of years, and recent policy changes by the Environmental Protection Agency have placed emphasis upon the gaseous emissions that lead to the formation of particulate matter as small as 2.5 μm diameter. In this qualitative study, camphene, Δ3-carene, limonene, and α-terpinene were thermally degraded in the presence of air to determine the number and kind of oxidative degradation products that might be expected under drying conditions used in processing wood products. Various chromatographic methods were used to isolate the products for proof of structure by NMR and/or GC-MS. The degradation products resulted from dehydrogenations, epoxidations, double bond cleavages, allylic oxidations, and rearrangements. A number of compounds not previously associated with the thermal degradation of these terpenes were identified.

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