115881-56-6 Usage
General Description
N-(2-Furylmethyl)-2-methylpropan-2-amine is a chemical compound that belongs to the class of organic compounds known as Furanones. These are compounds containing a furan ring, which is a five-membered aromatic ring with one oxygen atom and in this case, substituted by a methyl group. The systematic name of this compound is also known as N-(Furan-2-ylmethyl)-2-methylpropan-2-amine. N-(2-FURYLMETHYL)-2-METHYLPROPAN-2-AMINE is likely to be used in the field of organic synthesis for the production of a range of chemical products. Information about its physical and chemical properties such as melting point, boiling point, specific rotation, and toxicity is currently not available; therefore, care should be taken when handling this compound until comprehensive safety data is provided.
Check Digit Verification of cas no
The CAS Registry Mumber 115881-56-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,8,8 and 1 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 115881-56:
(8*1)+(7*1)+(6*5)+(5*8)+(4*8)+(3*1)+(2*5)+(1*6)=136
136 % 10 = 6
So 115881-56-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H15NO/c1-9(2,3)10-7-8-5-4-6-11-8/h4-6,10H,7H2,1-3H3
115881-56-6Relevant articles and documents
Parallel Kinetic Resolution of Intramolecular Furan Diels-Alder Cycloadducts via Asymmetric Hydroboration
Fulgheri, Tamara,Cornwall, Philip,Turner, Andrew R.,Sweeney, Joseph B.,Gill, Duncan M.
, p. 7223 - 7227 (2019)
We report parallel kinetic resolution of intramolecular Diels-Alder cycloadducts, where up to five stereocentres are defined using asymmetric hydroboration as the enantiodiscriminating reaction, and reveal evidence for dynamic kinetic resolution based on a reversible cycloaddition.
Aryne cycloaddition with 3-oxidopyridinium species
Ren, Hailong,Wu, Chunrui,Ding, Xiuxiu,Chen, Xiaoge,Shi, Feng
supporting information, p. 8975 - 8984,10 (2012/12/12)
The [3 + 2] cycloaddition of arynes with 3-oxidopyridinium species is examined using the Kobayashi benzyne precursor. The reaction affords a bicyclo[3.2.1] skeleton under mild conditions. A [7 + 2] cycloaddition mode with a subsequent pyridine ring-opening event has also been observed.
