42607-20-5 Usage
Uses
Used in Pharmaceutical Industry:
2,2'-DIMETHYL-THIAZOLIDINE-4-CARBOXYLIC ACID is used as a starting material for the synthesis of 2-?substituted-?3-?acetyl-?thiazolidine-?4-?carbonyl-?amino acid derivatives. These derivatives exhibit antibacterial and antifungal properties, making them valuable in the development of new drugs and treatments for various infections.
Used in Chemical Synthesis:
2,2'-DIMETHYL-THIAZOLIDINE-4-CARBOXYLIC ACID can be utilized as a building block in the synthesis of various complex organic molecules. Its unique structure and reactivity make it a versatile component in the creation of novel compounds with potential applications in different industries, such as pharmaceuticals, agrochemicals, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 42607-20-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,6,0 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 42607-20:
(7*4)+(6*2)+(5*6)+(4*0)+(3*7)+(2*2)+(1*0)=95
95 % 10 = 5
So 42607-20-5 is a valid CAS Registry Number.
42607-20-5Relevant academic research and scientific papers
[4R]-3-(Omega-AROYLPROPIONYL)-4-THIAZOLIDINECARBOXYLIC ACIDS AND ESTERS
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, (2008/06/13)
This disclosure describes novel 4R!-3-(ω-aroylpropionyl)-4-thiazolidinecarboxylic acids and esters and the cationic salts thereof which are useful as hypotensive agents in mammals.
Substituted azetidin-2-one antibiotics
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, (2008/06/13)
Monocyclic β-lactam antibiotics of the formula STR1 WHEREIN R is amino or acylamino, e.g., phenylacetylamino, phenylglycylamino and 2-[4-(3-amino-3-carboxypropoxy)phenyl]-2-hydroximinoacetylamino; R1 is H or ester forming group; R2 is H, --OCH3, --SCH3, or --CH3 ; and R3 is H or acetoxy; are useful antibacterials for controlling β-lactamase producing gram-negative bacteria and other pathogens. Intermediates useful in the preparation of the antibiotics and a novel process for preparing 4α-acetoxy substituted azetidin-2-ones are provided.