156892-82-9 Usage
Description
Benzyl N-(2-amino-2-methylpropyl)carbamate, also known as Carbapenem-1, is a synthetic chemical compound with potential therapeutic applications. It is a carbamate derivative containing a benzyl group, an amino group, and a carbapenem core. Benzyl N-(2-amino-2-methylpropyl)carbamate has been studied for its antimicrobial properties and potential use as an antibiotic. It is known for its broad-spectrum activity against a variety of bacteria, including carbapenem-resistant strains. Benzyl N-(2-amino-2-methylpropyl)carbamate shows promise as a potential treatment for bacterial infections, especially those caused by multidrug-resistant pathogens. Its chemical structure and properties make it a promising candidate for further research and development in the field of antimicrobial therapy.
Uses
Used in Pharmaceutical Industry:
Benzyl N-(2-amino-2-methylpropyl)carbamate is used as an antimicrobial agent for its broad-spectrum activity against various bacteria, including carbapenem-resistant strains. It is particularly useful for treating bacterial infections caused by multidrug-resistant pathogens, offering a potential solution to the growing problem of antibiotic resistance.
Used in Research and Development:
Benzyl N-(2-amino-2-methylpropyl)carbamate is used as a candidate for further research and development in the field of antimicrobial therapy. Its unique chemical structure and properties make it a valuable subject for studying new approaches to combat bacterial infections and developing novel antibiotics.
Check Digit Verification of cas no
The CAS Registry Mumber 156892-82-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,8,9 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 156892-82:
(8*1)+(7*5)+(6*6)+(5*8)+(4*9)+(3*2)+(2*8)+(1*2)=179
179 % 10 = 9
So 156892-82-9 is a valid CAS Registry Number.
156892-82-9Relevant articles and documents
Tricyclic compound, pharmaceutical composition and application thereof
-
Paragraph 0135; 0146-0148, (2021/08/07)
The present invention provides a tricyclic compound, an isomer thereof, a pharmaceutically acceptable salt, a pharmaceutical composition and an application thereof. The tricyclic compound has a structure represented by formula I, has a significant effect of inhibiting RET kinase activity, can effectively inhibit cancer cell proliferation, can be used as an RET kinase inhibitor, can be used for preparing medicines for treating RET kinase-mediated diseases, has a good treatment effect on RET kinase-mediated cancers and other diseases, and has a wide application prospect.
Inducing achiral aliphatic oligoureas to fold into helical conformations
Wechsel, Romina,Maury, Julien,Fremaux, Juliette,France, Scott P.,Guichard, Gilles,Clayden, Jonathan
supporting information, p. 15006 - 15009 (2014/12/11)
The ability of urea-linked oligomers of achiral diamines (achiral analogues of the well-established chiral oligourea foldamers) to adopt helical conformations was explored spectroscopically. Up to four achiral units were ligated either to a well-formed helical trimer or to a single chiral diamine, and the extent to which they adopted a screw-sense preference was determined by NMR and CD. In the best performing cases, a trimeric chiral oligourea and even a single cis-cyclohexanediamine monomer induced folding into a helical conformation.
MONO carbamate protection of aliphatic diamines using alkyl phenyl carbonates [(2-Aminoethyl)carbamic acid tert-butyl ester]
Pittelkow, Michael,Lewinsky, Rasmus,Christensen, J?rn B.,Cesario, Cara,Miller, Marvin J.
, p. 209 - 214 (2017/09/07)
-