165522-04-3 Usage
General Description
1,3-Dioxolane-4-carboxamide, 2,2-dimethyl-(9CI) is a chemical compound with the molecular formula C6H11NO2. It is a derivative of dioxolane and has a carboxamide functional group and two methyl groups attached to the carbon atom. 1,3-Dioxolane-4-carboxamide,2,2-dimethyl-(9CI) has potential applications in pharmaceutical and industrial settings due to its unique chemical structure. It may be used as a building block for the synthesis of new compounds with desirable properties, or as a component in the production of certain medications. Further research and testing may be necessary to fully understand the potential uses and properties of this chemical.
Check Digit Verification of cas no
The CAS Registry Mumber 165522-04-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,5,5,2 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 165522-04:
(8*1)+(7*6)+(6*5)+(5*5)+(4*2)+(3*2)+(2*0)+(1*4)=123
123 % 10 = 3
So 165522-04-3 is a valid CAS Registry Number.
165522-04-3Relevant articles and documents
Concise synthesis of enantiomers of 4-aminobutane-1,2,3-triol
Dunlap, Norma K.,Drake, John,Ward, Andrea,Salyard, Tracy L. J.,Martin, Leah
, p. 2928 - 2930 (2008/09/19)
(Chemical Equation Presented) A very efficient synthesis of (2R,3S) and (2S,3R)-4-aminobutane-1,2,3-triol has been developed using either D- or L-glucose as the starting material. A key step is the one-pot conversion of an aldehyde to an amide, the scope of which has been extended to include other carbohydrate-derived aldehydes.
1,3-dioxolane C-nucleosides: Asymmetric synthesis of four stereoisomers of 2-[2-(hydroxymethyl)-1,3-dioxolan-5-yl]-1,3-thiazole-4-carboxamide
Jinfa, Du,Fucheng, Qu,Lee Doo-won,Gary Newton,Chu Chung
, p. 8167 - 8170 (2007/10/02)
Asymmetric synthesis of four novel C-nucleosides, (2′R,5′R)-, (2′S,5′R)-, (2′S,5′S)- and (2′R,5′S)-2-[2-hydroxymethyl)-1,3-dioxolan-5-yl]-1,3-thiazole-4- carboxamide has been accomplished by the condensation of key intermediates, 2-(1R- and 1S-glycol-1-yl)-4-ethoxycarbonyl-1,3-thiazole with 2-benzoyloxy acetaldehyde dimethyl acetal.
