116607-29-5 Usage
Description
.beta.-D-Gulopyranose, 1,6-anhydro-3-deoxy-3-nitrois a chemical compound derived from a six-carbon sugar, specifically a derivative of gulopyranose. .beta.-D-Gulopyranose, 1,6-anhydro-3-deoxy-3-nitrofeatures a nitro group attached to it, which can influence its reactivity and properties. It holds significance in the realm of organic chemistry and serves as a potential building block for more complex compounds.
Uses
Used in Organic Chemistry:
.beta.-D-Gulopyranose, 1,6-anhydro-3-deoxy-3-nitrois used as a building block for [creating complex organic molecules] due to [its unique structure and the presence of the nitro group, which can participate in various chemical reactions].
Used in Chemical Synthesis:
In the field of chemical synthesis, .beta.-D-Gulopyranose, 1,6-anhydro-3-deoxy-3-nitrois used as a reagent for [synthesizing other organic molecules] because of [its ability to undergo specific reactions due to the nitro group, leading to the formation of desired products].
Used in Pharmaceutical Industry:
.beta.-D-Gulopyranose, 1,6-anhydro-3-deoxy-3-nitromay be used as an intermediate in the development of [pharmaceutical compounds] for [targeting specific biological pathways or creating novel drug candidates].
Used in Research and Development:
In the research and development sector, .beta.-D-Gulopyranose, 1,6-anhydro-3-deoxy-3-nitrois utilized as a compound for [exploring its properties and potential applications] in order to [gain insights into its reactivity and possible uses in various chemical processes].
Check Digit Verification of cas no
The CAS Registry Mumber 116607-29-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,6,0 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 116607-29:
(8*1)+(7*1)+(6*6)+(5*6)+(4*0)+(3*7)+(2*2)+(1*9)=115
115 % 10 = 5
So 116607-29-5 is a valid CAS Registry Number.
116607-29-5Relevant articles and documents
Synthesis studies of structural analogues of tagetitoxin: 4-O-acetyl-3- amino-1,6-anhydro-3-deoxy-D-gulose 2-phosphate
Dent, Barry R.,Furneaux, Richard H.,Gainsford, Graeme J.,Lynch, Gregory P.
, p. 6977 - 6996 (2007/10/03)
Synthetic approaches to structural analogues of tagetitoxin (1) are described. The successful route to analogue 3 (X=O) has, as a key step, protection of the cis-vicinal amino alcohol moiety of compound 7 as an N- benzylated cyclic carbamate (9). X-Ray cr
