185116-26-1 Usage
Chemical class
Thiadiazole-3-carboxylic acid derivative
Structure
Contains a 4-[(2-mercaptoethyl)amino] group
Potential applications
Pharmaceutical
Medicinal properties
May interact with biological systems and exhibit pharmacological activity
Molecular structure
Suggests the capability of forming complex interactions with protein targets in the body
Drug development
Potentially valuable compound for drug development and discovery
Research status
Further research is needed to explore its full range of potential therapeutic applications
Chemical identification
9CI (Chemical Abstracts Service Registry Number)
Functional groups
Thiadiazole ring, carboxylic acid, and 2-mercaptoethylamine
Chemical reactivity
May be influenced by the presence of the thiadiazole ring, carboxylic acid, and 2-mercaptoethylamine groups in its structure
Solubility
Not specified, but may be influenced by the presence of the carboxylic acid and thiol groups
Stability
Not specified, but may be affected by factors such as temperature, pH, and exposure to light or air
Toxicity
Not specified, but should be evaluated as part of its pharmaceutical development process
Synonyms
Not provided, but may exist under different names or trade names in the scientific literature or industry
Purity
Not specified, but should be determined and maintained to ensure the compound's effectiveness and safety in potential applications
Check Digit Verification of cas no
The CAS Registry Mumber 185116-26-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,5,1,1 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 185116-26:
(8*1)+(7*8)+(6*5)+(5*1)+(4*1)+(3*6)+(2*2)+(1*6)=131
131 % 10 = 1
So 185116-26-1 is a valid CAS Registry Number.
185116-26-1Relevant articles and documents
Synthesis of new macrocyclic lactams, lactones, and thiolactones
Yavolovskii,Ivanov,Ivanov
, p. 975 - 978 (1996)
A general method has been developed for the preparation of 14-membered cyclic lactams, lactones, and thiolactones from heteroaromatic amino acids. 1997 Plenum Publishing Corporation.
