34283-85-7 Usage
Uses
Used in Pharmaceutical Synthesis:
(4,5-DIHYDRO-1 H-IMIDAZOL-2-YLSULFANYL)-ACETIC ACID is used as a key intermediate in the synthesis of various pharmaceuticals for its unique chemical properties and reactivity.
Used in Organic Chemistry:
In the field of organic chemistry, (4,5-DIHYDRO-1 H-IMIDAZOL-2-YLSULFANYL)-ACETIC ACID is used as a reagent to facilitate specific chemical reactions and transformations.
Used in Cardiovascular Applications:
(4,5-DIHYDRO-1 H-IMIDAZOL-2-YLSULFANYL)-ACETIC ACID is used as a potential therapeutic agent for cardiovascular disorders, leveraging its ability to regulate blood pressure.
Used in Metabolic Disorders Treatment:
In metabolic disorder treatment, (4,5-DIHYDRO-1 H-IMIDAZOL-2-YLSULFANYL)-ACETIC ACID is used to help manage blood glucose levels, contributing to the treatment of conditions like diabetes.
Used in Anti-Inflammatory Applications:
(4,5-DIHYDRO-1 H-IMIDAZOL-2-YLSULFANYL)-ACETIC ACID is used as an anti-inflammatory agent, potentially reducing inflammation in various conditions.
Used in Antioxidant Applications:
As an antioxidant, (4,5-DIHYDRO-1 H-IMIDAZOL-2-YLSULFANYL)-ACETIC ACID is used to combat oxidative stress and related cellular damage.
Used in Research and Development:
In the research and development industry, (4,5-DIHYDRO-1 H-IMIDAZOL-2-YLSULFANYL)-ACETIC ACID is used to explore its potential biological and therapeutic effects, furthering our understanding of its capabilities and limitations in medical and chemical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 34283-85-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,2,8 and 3 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 34283-85:
(7*3)+(6*4)+(5*2)+(4*8)+(3*3)+(2*8)+(1*5)=117
117 % 10 = 7
So 34283-85-7 is a valid CAS Registry Number.
InChI:InChI=1/C5H8N2O2S/c8-4(9)3-10-5-6-1-2-7-5/h1-3H2,(H,6,7)(H,8,9)
34283-85-7Relevant academic research and scientific papers
New data on the alkylation of cyclic thioureas with α-halocarboxylic acids and their esters. 1. Alkylation of ethylene thiourea
Kushakova,Ramsh,Garabadgiu
, p. 221 - 226 (2007/10/03)
The detailed scheme of reactions, occurring on interacting ethylene thiourea with chloroacetic acid and its esters, has been supplemented with a series of new reactions. The whole spectrum of products formed on interaction of ethylene thiourea with 2-bromobutyric acid has been obtained. 2006 Springer Science+Business Media, Inc.
