87471-10-1 Usage
Imidazole class
1H-Imidazole-4-carboxaldehyde, 5-nitro-1-(phenylmethyl)belongs to the imidazole class of chemicals, which is a group of organic compounds that contain a five-membered ring with four carbon atoms and one nitrogen atom.
Imidazole ring
The compound consists of an imidazole ring, which is a five-membered ring with four carbon atoms and one nitrogen atom.
5-Nitro group
The compound has a 5-nitro group attached to the imidazole ring, which makes it useful in the synthesis of nitroimidazoles.
Phenylmethyl group
The compound also has a phenylmethyl group attached to the imidazole ring, which provides opportunities for further modification of the compound's structure.
Building block in organic synthesis
1H-Imidazole-4-carboxaldehyde, 5-nitro-1-(phenylmethyl)is commonly used as a building block in organic synthesis.
Used in pharmaceuticals and agrochemicals
The compound is particularly used in the creation of pharmaceuticals and agrochemicals.
Antibacterial and antiparasitic agents
Nitroimidazoles, which can be synthesized using this compound, are often used as antibacterial and antiparasitic agents.
Versatile chemical
1H-Imidazole-4-carboxaldehyde, 5-nitro-1-(phenylmethyl)is a versatile chemical that plays a significant role in the development of various important compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 87471-10-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,4,7 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 87471-10:
(7*8)+(6*7)+(5*4)+(4*7)+(3*1)+(2*1)+(1*0)=151
151 % 10 = 1
So 87471-10-1 is a valid CAS Registry Number.
87471-10-1Relevant articles and documents
Vicarious nucleophilic substitution of 1-benzyl-5-nitroimidazole, application to the synthesis of 6,7-dihydroimidazo[4,5-d][1,3]diazepin-8(3H)-one
Chen, Bang-Chi,Chao, Sam T.,Sundeen, Joseph E.,Tellew, John,Ahmad, Saleem
, p. 1595 - 1596 (2007/10/03)
Reaction of 1-benzyl-5-nitroimidazole with carbanion generated from chloroform and potassium tert-butoxide afforded 1-benzyl-4-dichloromethyl-5-nitroimidazole in 72% yield. This vicarious nucleophilic substitution reaction was successfully applied to the synthesis of 6,7-dihydroimidazo[4,5-d][1,3]diazepin-8(3H)-one, an important intermediate in the synthesis of natural and biologically active compounds.
