119139-25-2

Basic information

• Product Name: (Z)-1-{(5Z)-1-benzyl-5-[(2,2-diethoxyethyl)imino]-1,5-dihydro-4H-imidazol-4-ylidene}-N-ethoxymethanediamine
• CAS NO: 119139-25-2
• Molecular Formula: C₁₉H₂₉N₅O₃
• Molecular Weight: 375.4653
• Mol File: 119139-25-2.mol

Chemical Properties

• Boiling Point: 433.4°C at 760 mmHg
• Flash Point: 215.9°C
• Density: 1.17g/cm³
• Vapor Pressure: 1.03E-07mmHg at 25°C
• Refractive Index: 1.561
• CAS DataBase Reference: (Z)-1-{(5Z)-1-benzyl-5-[(2,2-diethoxyethyl)imino]-1,5-dihydro-4H-imidazol-4-ylidene}-N-ethoxymethanediamine(CAS DataBase Reference)
• NIST Chemistry Reference: (Z)-1-{(5Z)-1-benzyl-5-[(2,2-diethoxyethyl)imino]-1,5-dihydro-4H-imidazol-4-ylidene}-N-ethoxymethanediamine(119139-25-2)
• EPA Substance Registry System: (Z)-1-{(5Z)-1-benzyl-5-[(2,2-diethoxyethyl)imino]-1,5-dihydro-4H-imidazol-4-ylidene}-N-ethoxymethanediamine(119139-25-2)

Safety Data

• Hazardous Substances Data: 119139-25-2(Hazardous Substances Data)

Usage

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.

Upstream product

• 119139-24-1 1-benzyl-5--N'-ethoxy-1H-imidazole-4-carboxamidine 
• 70276-43-6 1-Benzyl-N'-ethoxy-5-formamido-1H-imidazole-4-carboxamidine 
• 51806-20-3 1,1-diethoxy-2-iodoethane 

Downstream Products

• 119139-26-3 1-Benzyl-5-(2,2-diethoxy-ethylamino)-1H-imidazole-4-carboxamidine 
• 161975-87-7 3-benzylazepinomycin 
• 119139-27-4 1-benzyl-5-(2,2-diethoxyethylamino)-1H-imidazole-4-carboxamide 

Relevant 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

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.

ALTERNATIVE SYNTHESES OF AZEPINOMYCIN

Three alternative syntheses of the antibiotic azepinomycin (XI) have now become feasible through a route starting from the monocycles Va-c and proceeding through the intermediates VIa-c, VIIa-c, VIIIa-c, IXa-c, and XIIa,b and 3-β-D-ribofuranosylazepinomycin (XIIc). The permutation IXa-Xa-XI was also found to be feasible. The starting materials Va-c were readily prepared from IIa-c through IIIa-c and IVa-c.