Название продукции:cis-N1-Boc-1,2-cyclopentanediamine

IUPAC Name:tert-butyl N-[(1R,2S)-2-aminocyclopentyl]carbamate

CAS:365996-19-6
Молекулярная формула:C10H20N2O2
Чистота:95%
Номер в каталоге:CM117933
Молекулярная масса:200.28

Упаковочная единица Доступно для заказа Цена ($) Количество
CM117933-1g 4-5 Weeks ƴƏţ

Только для использования в НИОКР..

Форма запроса

   refresh    

Информация о продукции

Номер CAS:365996-19-6
Молекулярная формула:C10H20N2O2
Точка плавления:-
Smiles-код:N[C@@H]1[C@H](NC(OC(C)(C)C)=O)CCC1
Плотность:
Номер в каталоге:CM117933
Молекулярная масса:200.28
Точка кипения:
Номер Mdl:MFCD12197288
Хранение:

Category Infos

Cyclopentanes
Cyclopentane is a cycloalkane, an organic compound with a molecular formula of C5H10, a colorless and transparent liquid, insoluble in water, soluble in most organic solvents such as ethanol, ether, benzene, carbon tetrachloride, acetone, etc. It is mainly used as a solvent and chromatographic reference materials.
Cyclopentanes,where to buy Cyclopentanes
Cyclopentanes
Cyclopentane (also called C pentane) is a highly flammable alicyclic hydrocarbon with chemical formula C5H10 and CAS number 287-92-3, consisting of a ring of five carbon atoms each bonded with two hydrogen atoms above and below the plane. It occurs as a colorless liquid with a petrol-like odor.

Column Infos

Cyclanes
Cyclanes are secondary metabolites that can be found in plants, and are also biochemicals that can be used in medicine. Cyclanes are found in pine trees, and are used in the making of plastics. Cyclenes are found in cinnamon, and have antifungal properties.

Related Products



Product Other Information

Product Overview Tert-Butyl ((1R,2S)-2-aminocyclopentyl)carbamate, also known as Boc-aminocyclopentane, is a chemical compound used in scientific research. It is a derivative of cyclopentane and is commonly used as a protecting group for amino acids during peptide synthesis. 
Synthesis Method Tert-Butyl ((1R,2S)-2-aminocyclopentyl)carbamate can be synthesized using several methods. One of the most common methods is the reaction of tert-butyl carbamate with (1R,2S)-2-aminocyclopentanol in the presence of a catalyst. Another method involves the reaction of tert-butyl carbamate with (1R,2S)-2-aminocyclopentanone in the presence of a reducing agent.
Chemical Properties It allows for the selective protection of the amino group, which is important for the synthesis of complex peptides. It also allows for the synthesis of peptides with high yields and purity.However, there are also limitations to its use. The removal of the protecting group can be difficult and may require harsh conditions, which can lead to unwanted side reactions. It may also be incompatible with certain reaction conditions, limiting its use in some peptide synthesis reactions.
Synthesis and Application Tert-Butyl ((1R,2S)-2-aminocyclopentyl)carbamate is widely used in scientific research, particularly in peptide synthesis. It is commonly used as a protecting group for amino acids during peptide synthesis. It can also be used as a reagent for the preparation of chiral amines and as a starting material for the synthesis of various biologically active compounds.
Future Directions One direction is the development of new methods for the selective removal of the protecting group. Another direction is the synthesis of new peptides and biologically active compounds using tert-Butyl ((1R,2S)-2-aminocyclopentyl)carbamate as a starting material. Additionally, the use of tert-Butyl ((1R,2S)-2-aminocyclopentyl)carbamate in the synthesis of complex peptides and proteins may have important applications in drug discovery and development.