102635-15-4 Usage
Structure
A triazine ring with three ketone groups attached (1,3,5-triazine-2,4,6(1H,3H,5H)-trione)
Derivative of
Uracil
Functional groups
Ketone groups, triazine ring, and an acetyl group
Reactivity
High reactivity due to the presence of multiple functional groups
Applications
a. Organic synthesis
b. Building block for pharmaceuticals and agrochemicals
c. Reagent in various chemical reactions
d. Starting material for the synthesis of heterocyclic compounds
Potential uses
Medicine, materials science, and biochemical research
Check Digit Verification of cas no
The CAS Registry Mumber 102635-15-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,6,3 and 5 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 102635-15:
(8*1)+(7*0)+(6*2)+(5*6)+(4*3)+(3*5)+(2*1)+(1*5)=84
84 % 10 = 4
So 102635-15-4 is a valid CAS Registry Number.
102635-15-4Relevant articles and documents
Reactions of Carbonyl Diisocyanate with Amides and Acids
Akteries, Bernhard,Jochims, Johannes C.
, p. 669 - 682 (2007/10/02)
Carbonyl diisocyanate (1) reacts with primary amides to give 1-acylated isocyanuric acids (5, 6).With secondary amides, 1 affords the rather instable oxadiazinediones 4, which for certain substituents rearrange to give triazines (5, 10).With nucleophiles, compounds 4 give oligourets, e.g. with ureas pentaurets (11, 12) were obtained.Carbonyl diisocyanate reacts with hydrogen halides to afford the crystalline urea-1,3-dicarbonyl halides 13a-c.Diverse products (16, 17, 24, 26) were obtained with carboxylic acids.In most cases oxadiazinediones (26) were isolated, which can be transformed with nucleophiles into acyl ureas 30, 31, biurets 32, and triurets 33.Acetylation of 26 leads to the reactive heterocycles 34.
