18221-88-0 Usage
General Description
Glycollylguanidine, also known as glyceryl guanidine, is a chemical compound that consists of guanidine, an important part in the formation of urea, in combination with glycol, a dihydric alcohol. The specific implications and uses of this chemical vary, with potential functional uses in various industries. However, detailed information about this compound including its structure, properties, spectra, suppliers, and links for its literature in various databases are not widely available, suggesting that it may not be commonly used or extensively studied. As such, it is essential to carry out appropriate tests and experiments following established safety protocols to understand its impacts and potential uses fully.
Check Digit Verification of cas no
The CAS Registry Mumber 18221-88-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,2,2 and 1 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 18221-88:
(7*1)+(6*8)+(5*2)+(4*2)+(3*1)+(2*8)+(1*8)=100
100 % 10 = 0
So 18221-88-0 is a valid CAS Registry Number.
18221-88-0Relevant articles and documents
An efficient approach to dispacamide A and its derivatives
Guiheneuf, Solene,Paquin, Ludovic,Carreaux, Francois,Durieu, Emilie,Meijer, Laurent,Bazureau, Jean Pierre
, p. 978 - 987 (2012)
Dispacamide A and new analogs of this marine alkaloid were prepared in seven steps with an overall yield ranging from 12 to 33%. The key step of the strategy was a stereocontrolled Knoevenagel condensation under microwave dielectric heating in the last step. In this condensation, the 2-aminoimidazolin-4-one hydrochloride partners 10a-c were synthesized in three steps with good overall yields (33-79%) via the ring closure of N-guanidino acetic acids 9a-c and the aldehydes 5a,b as the two others building-blocks, in 3 steps with 60-66% overall yields. The six synthetic products have been obtained with a Z geometry about their exocyclic bond on the basis of 13C/1H long-range coupling constants using a gHSQMBC experiment.
