119139-25-2 Usage
Description
(Z)-1-(5Z)-1-benzyl-5-[(2,2-diethoxyethyl)imino]-1,5-dihydro-4H-imidazol-4-ylidene-N-ethoxymethanediamine is a complex organic compound derived from the imidazole family. It features a benzyl group and an N-ethoxymethanediamine group, along with diethoxyethyl and imino moieties. The unique molecular structure and composition of this compound make it a versatile molecule with potential applications in various fields, including pharmaceuticals, materials science, and organic chemistry. Further research and analysis are required to explore its full potential and properties.
Uses
Used in Pharmaceutical Applications:
(Z)-1-(5Z)-1-benzyl-5-[(2,2-diethoxyethyl)imino]-1,5-dihydro-4H-imidazol-4-ylidene-N-ethoxymethanediamine is used as a building block for the development of novel pharmaceutical compounds due to its unique chemical structure and reactivity. Its ability to participate in various chemical reactions allows for the synthesis of new drugs with potential therapeutic applications.
Used in Materials Science:
In the field of materials science, (Z)-1-(5Z)-1-benzyl-5-[(2,2-diethoxyethyl)imino]-1,5-dihydro-4H-imidazol-4-ylidene-N-ethoxymethanediamine is used as a component in the creation of advanced materials with specific properties. Its incorporation into polymers or other materials can lead to the development of new materials with enhanced characteristics, such as improved stability, reactivity, or selectivity.
Used in Organic Chemistry:
(Z)-1-(5Z)-1-benzyl-5-[(2,2-diethoxyethyl)imino]-1,5-dihydro-4H-imidazol-4-ylidene-N-ethoxymethanediamine serves as a valuable intermediate in organic synthesis. Its unique structure allows for its use in the synthesis of various organic compounds, potentially leading to the development of new molecules with diverse applications in various industries.
Used in Chemical Research:
(Z)-1-(5Z)-1-benzyl-5-[(2,2-diethoxyethyl)imino]-1,5-dihydro-4H-imidazol-4-ylidene-N-ethoxymethanediamine is also used as a research tool in the field of chemistry. Its complex structure and reactivity make it an interesting subject for studying reaction mechanisms, exploring new synthetic routes, and understanding the fundamental principles of chemical reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 119139-25-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,1,3 and 9 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 119139-25:
(8*1)+(7*1)+(6*9)+(5*1)+(4*3)+(3*9)+(2*2)+(1*5)=122
122 % 10 = 2
So 119139-25-2 is a valid CAS Registry Number.
119139-25-2Relevant articles and documents
Purines. LXIII. Syntheses of azepinomycin, an antitumor antibiotic from Streptomyces species, and its 3-β-D-ribofuranoside and their 8-imino analogues
Fujii,Saito,Fujisawa
, p. 1231 - 1237 (2007/10/02)
Three variants of a synthetic route to the antitumor antibiotic azepinomycin (3) from 1-substituted N'-alkoxy-5-formamidoimidazole-4- carboxamidine (type 10) are described. The synthesis started with the monocycles 10a-c and proceeded through the intermediates 11a-c, 12a-c, 13a- c, 14a-c, and 4a, b and 3-β-D-ribofuranosylazepinomycin (4c). The benzyl version (series a), including the permutation 14a → 15 → 3, was found to produce the antibiotic (3) most efficiently. The starting materials 10a-c were readily prepared from the 9-substituted adenines 7a-c via the N-oxides 8a-c and the 1-alkoxy derivatives 9a-c. The 8-imino analogues (17 and 18) of 3 and 4c were also synthesized from 12a and 12c, respectively.
