410090-37-8 Usage
Uses
Used in Organic Synthesis:
cis-3-[(tert-Butoxycarbonyl)amino]cyclopentane-1-carboxylic acid, tert-Butyl (cis-3-carboxycyclopent-1-yl)carbamate is used as a synthetic intermediate for the creation of complex organic molecules. Its carboxylic acid group allows for the formation of esters, amides, and other functional groups, facilitating the synthesis of a wide range of compounds with diverse properties.
Used in Drug Discovery Research:
In the pharmaceutical industry, cis-3-[(tert-Butoxycarbonyl)amino]cyclopentane-1-carboxylic acid, tert-Butyl (cis-3-carboxycyclopent-1-yl)carbamate is used as a key component in the development of new drugs. Its unique structure and functional groups make it a promising candidate for the design of bioactive molecules with potential therapeutic applications.
Used as a Protecting Group in Amino Acid Chemistry:
cis-3-[(tert-Butoxycarbonyl)amino]cyclopentane-1-carboxylic acid, tert-Butyl (cis-3-carboxycyclopent-1-yl)carbamate is used as a protecting group for amino acids during peptide synthesis. The tert-butyl carbamate group can be selectively removed under mild conditions, allowing for the controlled assembly of peptide sequences and the synthesis of complex peptide-based drugs.
Used in the Synthesis of Proline Derivatives:
As a derivative of proline, cis-3-[(tert-Butoxycarbonyl)amino]cyclopentane-1-carboxylic acid, tert-Butyl (cis-3-carboxycyclopent-1-yl)carbamate is used in the synthesis of various proline analogs and derivatives. These modified amino acids can be incorporated into peptides and proteins to study their effects on protein structure and function, as well as to develop new bioactive peptides and peptidomimetics.
Used in the Development of Chiral Compounds:
The chiral center present in cis-3-[(tert-Butoxycarbonyl)amino]cyclopentane-1-carboxylic acid, tert-Butyl (cis-3-carboxycyclopent-1-yl)carbamate makes it a valuable starting material for the synthesis of enantiomerically pure compounds. These chiral compounds have applications in various fields, including asymmetric catalysis, enantioselective synthesis, and the development of chiral drugs with improved pharmacological properties.
Check Digit Verification of cas no
The CAS Registry Mumber 410090-37-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,1,0,0,9 and 0 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 410090-37:
(8*4)+(7*1)+(6*0)+(5*0)+(4*9)+(3*0)+(2*3)+(1*7)=88
88 % 10 = 8
So 410090-37-8 is a valid CAS Registry Number.
