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444772-06-9

3-Oxa-1-azaspiro[4.5]decan-2-one, 6-methoxy-, (5R,6S)-rel-(9CI) is a complex organic compound with the molecular formula C10H17NO3. It is a chiral molecule, meaning it has a non-superimposable mirror image, and it is characterized by its specific stereochemistry, with the (5R,6S) configuration. 3-Oxa-1-azaspiro[4.5]decan-2-one,6-methoxy-,(5R,6S)-rel-(9CI) features a spiro ring system, which consists of two rings sharing a common atom, in this case, a carbon atom. The molecule also contains a 3-oxa group, indicating the presence of an oxygen atom in a three-membered ring, and a 6-methoxy group, which is a methoxy group (-OCH3) attached to the sixth carbon atom. 3-Oxa-1-azaspiro[4.5]decan-2-one,6-methoxy-,(5R,6S)-rel-(9CI) is likely to be found in specialized chemical libraries or used in advanced organic synthesis due to its unique structure and potential applications in pharmaceuticals or chemical research.

444772-06-9

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  • 3-Oxa-1-azaspiro[4.5]decan-2-one,6-methoxy-,(5R,6S)-rel-(9CI)

    Cas No: 444772-06-9

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444772-06-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 444772-06-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,4,7,7 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 444772-06:
(8*4)+(7*4)+(6*4)+(5*7)+(4*7)+(3*2)+(2*0)+(1*6)=159
159 % 10 = 9
So 444772-06-9 is a valid CAS Registry Number.

444772-06-9Downstream Products

444772-06-9Relevant articles and documents

Rhodium(II)-catalyzed aziridination of allyl-substituted sulfonamides and carbamates

Padwa, Albert,Flick, Andrew C.,Leverett, Carolyn A.,Stengel, Thomas

, p. 6377 - 6386 (2007/10/03)

Several unsaturated sulfonamides underwent intramolecular aziridination when treated with PhI-(OAc)2, MgO, and catalytic Rh 2(OAc)4 to give bicyclic aziridines in excellent yield. Treatment of the resulting azabicyclic sul

Stereochemical aspects of the iodine(III)-mediated aziridination reaction of some cyclic allylic carbamates.

Padwa, Albert,Stengel, Thomas

, p. 2137 - 2139 (2007/10/03)

[reaction: see text] The iodine(III)-mediated aziridination reaction of an indolyl-substituted carbamate requires a Rh(II) catalyst and proceeds by a metallonitrene intermediate. Stepwise addition across the indole pi-bond followed by Rh(II) detachment ge

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