81366-70-3 Usage
General Description
2-Deoxy-N-phenyl-D-erytho-pentofuranosylamine is a unique chemical compound that belongs to a group known as monosaccharides, which are the simplest form of carbohydrates. The specific composition and arrangement of atoms in 2-Deoxy-N-phenyl-D-erytho-pentofuranosylamine make it of interest in fields such as biochemistry, where it might have potential uses or interactions with biological systems. However, as of now, detailed information about this chemical compound such as its biological activity, toxicity, and other chemical properties remains scarce in the literature. Further chemical, biological, and pharmaceutical research could potentially unfold the unknown characteristics and possible applications of this intriguing compound.
Check Digit Verification of cas no
The CAS Registry Mumber 81366-70-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,3,6 and 6 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 81366-70:
(7*8)+(6*1)+(5*3)+(4*6)+(3*6)+(2*7)+(1*0)=133
133 % 10 = 3
So 81366-70-3 is a valid CAS Registry Number.
81366-70-3Relevant articles and documents
Ni-catalyzed homoallylation of polyhydroxy N,O- Acetals with conjugated dienes promoted by triethylborane
Mori, Takamichi,Akioka, Yusuke,Onodera, Gen,Kimura, Masanari
supporting information, p. 9288 - 9306 (2014/08/05)
In the presence of Ni-catalyst and triethylborane, N,O- Acetals prepared from glycolaldehyde and glyceraldehyde with primary amines in situ underwent homoallylation with conjugated dienes to provide 2- Amino-5-hexenols in high regio- And stereoselectivity
THE CHEMISTRY OF O-SILYLATED KETENE ACETALS; DIASTEREOSELECTIVE ALDOL REACTION OF 2,3-O-ISOPROPYLIDENE-D (AND L)-GLYCERALDEHYDES LEADING TO 2-DEOXY-D (AND L)-RIBOSES
Kita, Yasuyuki,Yasuda, Hitoshi,Tamura, Osamu,Itoh, Fumio,Ke, Ya Yuan,Tamura, Yasumitsu
, p. 5777 - 5780 (2007/10/02)
Diastereoselective carbon-carbon bond forming reaction of 2,3-O-isopropylidene-D (and L)-glyceraldehydes (D and L-2) with ketene silyl acetals (1a,b) occured in acetonitrile under mild conditions to give the corresponding anti-β-siloxyesters (D and L-3a) as major products, which could be converted through a few additional steps to 2-deoxy-D (and L)-riboses.