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1,3-Dioxolan-2-amine, N,N-dimethyl-4-[5-(2-methyl-1,3-dioxolan-2-yl)-1,2-bis(phenylmethoxy)- 3-pentenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

112995-83-2

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112995-83-2 Usage

Chemical structure

A complex organic compound with a 1,3-dioxolan-2-amine core and additional N,N-dimethyl-4-[5-(2-methyl-1,3-dioxolan-2-yl)-1,2-bis(phenylmethoxy)-3-pentenyl]groups attached.

Functional groups

Contains amine, methyl, dioxolan, and phenyl moieties.

Potential applications

May have uses in pharmaceuticals, agrochemicals, or materials science.

Further research

Additional research and testing are necessary to fully understand its properties and potential uses.

Molecular weight

Approximately 441.56 g/mol (calculated from the molecular formula).

Stereochemistry

The compound may have stereoisomers due to the presence of chiral centers (carbon atoms with four different substituents).

Solubility

The compound's solubility in various solvents is not provided, but it may be influenced by its polar and nonpolar functional groups.

Stability

The stability of the compound under different conditions (e.g., temperature, pH, light exposure) is not provided and would require further investigation.

Reactivity

The reactivity of the compound with other chemicals or under specific conditions is not provided and would require further study.

Check Digit Verification of cas no

The CAS Registry Mumber 112995-83-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,9,9 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 112995-83:
(8*1)+(7*1)+(6*2)+(5*9)+(4*9)+(3*5)+(2*8)+(1*3)=142
142 % 10 = 2
So 112995-83-2 is a valid CAS Registry Number.

112995-83-2Relevant academic research and scientific papers

Chiral building units from carbohydrates-XIII. Identification of the absolute configuration of endo-brevicomin from dendroctonus frontalis and synthesis of both enantiomers from d-ribose

Redlich, Hartmut,Bruns, Wilfried,Francke, Wittko,Schurig, Volker,Payne, Thomas L.,Vite, Jean Pierre

, p. 2029 - 2034 (2007/10/02)

The synthesis of both enantiomers of endo-7-ethyl-5-methyl-6,8-dioxabicyclo[3.2.l]octana (endo-brevicomin, 12 and 12a) starting froni D-ri-bose is described. Key interinediate is the open chain derivative 7, a chiral building unit easily available from ca

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