42400-25-9 Usage
Dihydropyrimidine ring
A heterocyclic compound containing oxygen and nitrogen atoms.
Ethoxy group
A functional group consisting of an ethoxy unit (C2H5O-) that can participate in chemical reactions.
Hydroxy group
A polar functional group (-OH) that can form hydrogen bonds and participate in chemical reactions.
Aldehyde group
A carbonyl group (C=O) bonded to a hydrogen atom and a carbon atom, which can act as a reducing agent in certain reactions.
2-oxoethoxy
A functional group that contributes to the compound's reactivity and potential applications in synthetic chemistry.
3-hydroxypropanal
A part of the compound's structure that includes a hydroxy group and an aldehyde group, which can be involved in chemical reactions and contribute to the compound's properties.
Complex structure
The compound's intricate arrangement of atoms and functional groups, which can affect its reactivity and potential applications.
Synthetic chemistry value
The compound's potential use in the synthesis of new compounds and materials due to its complex structure and multiple functional groups.
Pharmaceutical research potential
The possibility that the compound may be used in the development of new drugs or therapeutic agents due to its unique properties and reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 42400-25-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,4,0 and 0 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 42400-25:
(7*4)+(6*2)+(5*4)+(4*0)+(3*0)+(2*2)+(1*5)=69
69 % 10 = 9
So 42400-25-9 is a valid CAS Registry Number.
42400-25-9Relevant articles and documents
Effective Synthesis of Fluorescently Labeled Morpholino Nucleoside Triphosphate Derivatives
Tarasenko, Yuliya V.,Abramova, Tatyana V.,Mamatuk, Viktor I.,Silnikov, Vladimir N.
, p. 32 - 42 (2016/02/19)
Morpholino nucleoside triphosphates (A, U, G, C, T) bearing the active functional amino group tethered to morpholine residue and their fluorescently labeled derivatives were synthesized. All compounds were characterized by 1H, 13C, a
Daunorubicin derivatives obtained from daunorubicin and nucleoside dialdehydes
Olsufyeva, Eugenia N.,Brusentsov, Nikolai A.,Todorova, Nedyalka,Balzarini, Jan,De Clercq, Erik,Preobrazhenskaya, Maria N.
, p. 87 - 95 (2007/10/03)
Nucleoside dialdehydes were obtained by periodate oxidation of adenosine, cytidine, guanosine, uridine or 6-azauridine in the presence of Dowex (1x8; CH3COO-). Reductive alkylation of daunorubicin with these dialdehydes in the presence of NaBH3CN produced a series of 3'-deamino-3'- (4-morpholino)daunorubicin or 13-(R,S)-dihydrodaunorubicin derivatives, the latter being mixtures of two diastereomers at 13-C atom. The morpholino- daunorubicin derivatives containing nucleic base moieties are less cytotoxic than cyanomorpholino-daunorubicin, morpholino-daunorubicin and even than the parent antibiotic.
NUCLEOSIDES. XXII. SYNTHESIS OF
WATANABE,FOX
, p. 975 - 976 (2007/10/07)
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