178979-59-4 Usage
Molecular structure
1-1-butyl-5-[(3,5-dichlorophenyl)sulfanyl]-4-(1-methylethyl)-1H-imidazol-2-ylmethanamine consists of a complex arrangement of atoms, including carbon, hydrogen, chlorine, nitrogen, and sulfur.
Functional groups
The compound contains a butyl group (a four-carbon alkyl chain), a sulfanyl group attached to a 3,5-dichlorophenyl group (which provides electrophilic properties), and an imidazol-2-yl group (a five-membered aromatic ring with two nitrogen atoms).
Methanamine moiety
A positively charged nitrogen atom is present in the form of a methanamine group (an amino group attached to a single carbon atom), which is connected to the imidazol-2-yl group.
Potential pharmacological properties
The compound may have biological activity and could be used in the development of medications or in research studies.
Complex structure
Due to the intricate arrangement of atoms and functional groups, the compound may exhibit unique chemical and physical properties.
Potential reactivity
The presence of reactive functional groups, such as the sulfanyl group, may lead to unwanted side reactions or decomposition under certain conditions.
Laboratory safety
The compound should be handled with caution in a laboratory setting due to its complex structure and potential reactivity. Proper safety precautions, such as wearing gloves and using a fume hood, should be followed when working with 1-{1-butyl-5-[(3,5-dichlorophenyl)sulfanyl]-4-(1-methylethyl)-1H-imidazol-2-yl}methanamine.
Check Digit Verification of cas no
The CAS Registry Mumber 178979-59-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,8,9,7 and 9 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 178979-59:
(8*1)+(7*7)+(6*8)+(5*9)+(4*7)+(3*9)+(2*5)+(1*9)=224
224 % 10 = 4
So 178979-59-4 is a valid CAS Registry Number.
178979-59-4Relevant academic research and scientific papers
Imidazole derivatives as anti-HIV agents
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, (2008/06/13)
An imidazole derivative represented by general formula (I) or a salt thereof, having the effect of specifically inhibiting the growth of HIV as a pathogenic virus and being reduced in toxicity. In said formula R1 represents hydrogen, C1 -C20 alkyl, C2 -C7 alkenyl, C4 -C12 cycloalkylalkyl, etc.; R2 represents C1 -C6 alkyl, C1 -C6 acyl, hydroxyiminomethyl, hydrazonomethyl or --(CH2)n--R4 (R4 being halogeno, alkoxy, hydroxy, etc.; and n being an integer of 1 to 3); R3 represents substituted or unsubstituted C1 -C6 alkyl; X and Y represent each independently hydrogen, C1 -C3 alkyl, halogeno, or nitro; and Z represents S, SO, SO2 or CH2. STR1
