102224-22-6 Usage
Description
(4S,5S)-5-(formylamino)-2,2-dimethyl-4-phenyl-1,3-dioxane is a complex organic compound characterized by its chiral configuration of (4S,5S) and the presence of a formylamino group, a dioxane ring, phenyl, and dimethyl groups. This unique molecular structure suggests potential applications in various fields, including pharmaceuticals and materials science.
Uses
Used in Pharmaceutical Industry:
(4S,5S)-5-(formylamino)-2,2-dimethyl-4-phenyl-1,3-dioxane is used as a potential pharmaceutical compound for its unique molecular structure and chiral configuration. (4S,5S)-5-(formylamino)-2,2-dimethyl-4-phenyl-1,3-dioxane's formylamino group and dioxane ring may offer specific interactions with biological targets, making it a candidate for the development of new drugs.
Used in Materials Science:
In the field of materials science, (4S,5S)-5-(formylamino)-2,2-dimethyl-4-phenyl-1,3-dioxane could be utilized for the development of novel materials with specific properties. (4S,5S)-5-(formylamino)-2,2-dimethyl-4-phenyl-1,3-dioxane's structural features may contribute to the creation of materials with tailored characteristics for various applications, such as in coatings, adhesives, or polymers.
Further research and analysis are required to fully understand the potential applications and optimize the use of (4S,5S)-5-(formylamino)-2,2-dimethyl-4-phenyl-1,3-dioxane in these and other industries.
Check Digit Verification of cas no
The CAS Registry Mumber 102224-22-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,2,2 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 102224-22:
(8*1)+(7*0)+(6*2)+(5*2)+(4*2)+(3*4)+(2*2)+(1*2)=56
56 % 10 = 6
So 102224-22-6 is a valid CAS Registry Number.
102224-22-6Relevant articles and documents
AN IMPROVED SYNTHESIS OF (4S,5S)-2,2-DIMETHYL-4-PHENYL-1,3-DIOXAN-5-AMINE
Nordin, Ivan C.,Thomas, James A.
, p. 5723 - 5724 (1984)
The title compound is prepared in 78percent yield using an improved one-pot procedure which does not require final purification.
New chiral iminium salt catalysts for asymmetric epoxidation
Bulman Page, Philip C.,Buckley, Benjamin R.,Rassias, Gerasimos A.,Blacker, A. John
, p. 803 - 813 (2007/10/03)
A range of enantiomerically pure 4-substituted 5-amino-1,3-dioxanes has been condensed with 2-(2-bromoethyl)benzaldehyde to produce chiral dihydroisoquinolinium salts, which are effective asymmetric catalysts for the epoxidation of simple alkenes, giving ees of up to 71 %. Wiley-VCH Verlag GmbH & Co. KGaA, 2006.
