112094-14-1 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 19 carbon (C), 24 hydrogen (H), 6 nitrogen (N), 3 oxygen (O), and 1 sulfur (S) atoms.
Explanation
Benzimidazole is a heterocyclic compound with a fused benzene and imidazole ring. The compound in question is a derivative of benzimidazole, meaning it has additional functional groups or modifications to the core structure.
Explanation
Morpholine is a cyclic amine with a four-membered ring containing two carbon and two nitrogen atoms. The compound has two of these groups attached to the benzimidazole core.
Explanation
The nitro group is a functional group consisting of an oxygen-nitrogen-oxygen arrangement. It is known for its explosive properties and is often used in the synthesis of various compounds.
Explanation
The compound may have the ability to interact with biological systems, such as enzymes, receptors, or other cellular components, which could lead to potential applications in medicinal and pharmaceutical research.
Explanation
Due to its unique molecular structure and functional groups, the compound may be studied for its potential to develop new drugs or therapies for various medical conditions.
Explanation
The specific arrangement of atoms and the presence of functional groups in the compound contribute to its unique properties, which may be exploited in drug development and other fields of organic chemistry.
Explanation
The compound's unique properties and potential biological activities make it a candidate for further research and development in the creation of new drugs or therapies.
Explanation
The compound's unique structure and properties may be of interest to researchers in various subfields of organic chemistry, such as medicinal chemistry, synthetic chemistry, and chemical biology.
Benzimidazole derivative
A type of organic compound derived from benzimidazole
Contains two morpholine groups
Morpholine is a five-membered heterocyclic compound
Contains a nitro group
A functional group with the structure -NO2
Potential biological activities
Capable of interacting with biological systems
Used in medicinal and pharmaceutical research
Investigated for its potential therapeutic properties
Unique properties
Derived from its molecular structure and functional groups
Potential applications in drug development
May be used to create new therapeutic agents
Fields of organic chemistry
Applicable in various areas of chemical research and synthesis
Check Digit Verification of cas no
The CAS Registry Mumber 112094-14-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,0,9 and 4 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 112094-14:
(8*1)+(7*1)+(6*2)+(5*0)+(4*9)+(3*4)+(2*1)+(1*4)=81
81 % 10 = 1
So 112094-14-1 is a valid CAS Registry Number.
112094-14-1Relevant articles and documents
Synthesis of Substituted 2-Phenylbenzothiazoles and 5(6)-Nitro-1,3-disubstituted-benzimidazoline-2-thiones as CNS Active Agents.
Varma, Rajendra S.,Chauhan, Sudha,Prasad, C. R.
, p. 438 - 442 (2007/10/02)
p-(Benzothiazolyl)phenoxyacetylhydrazine (2), obtained by the hydrazinolysis of ethyl-p-(2-benzothiazolyl)phenoxyacetate (1), when reacted with salicylaldehyde gives N-(2-hydroxybenzylidene)-p-(2-benzothiazolyl)phenoxyacetylhydrazine (3).Condensation of isatin and N-methylisatin with 2 affords the corresponding hydrazones (4 and 5).The hydrazone 4 on Mannich reaction gives 6.Mannich reaction of benzoxazolin-2-one, benzoxazoline-2-thione and benzothiazoline-2-thione with 2-(p-aminophenyl)benzothiazole (7) furnishes 8, 9 and 10 respectively.Condensation of isatin and N-methylisatin with 7 gives 11 and 12 respectively.The Mannich condensation of 11 with morpholine/piperidine yields 13.Treatment of acetanthranil with 7 gives 14 which on reaction with benzaldehyde affords 3--2-styryl-4(3H)-quinazolinone (15). 1,3-Bis(amino/anilinomethyl)-5(6)-nitrobenzimidazoline-2-thiones (16) have been obtained by the Mannich condensation of 5(6)-nitrobenzimidazoline-2-thione with different amines/anilines.
