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1009075-44-8
Carbamic acid, N-[(1R,3R)-3-aminocyclopentyl]-, 1,1-dimethylethyl ester

Catalog#:1P0003MM

CAS:1009075-44-8

MDL:MFCD16037624

Molecular Formula:C10H20N2O2

Molecular Weight:200.2780

UN Number:

Haz Class:

Packing Group:

Synonyms: 1009075-44-8; 947732-58-3; ZINC36532969; AKOS025146858; SB21939; AJ-93126; AS-51070; trans-3-Amino-1-(Boc-amino)cyclopentane; t-Butyl [trans-3-aminocyclopentyl]carbamate; (1R,3R)-3-(Boc-amino)cyclopentan-1-amine; CS-0058567; KS-00000899; tert-Butyl ((1R,3R)-3-aminocyclopentyl)carbamate; A-6865; (3-Amino-cyclopentyl_carbamic acid tert-butyl ester; tert-butyl rac-[(1R,3R)-3-aminocyclopentyl]carbamate; ((1R,3R)-3-amino-cyclopentyl)-carbamic acid tert-butyl ester; Carbamic acid, N-[(1R,3R)-3-aminocyclopentyl]-, 1,1-dimethylethyl ester; tert-Butyl [trans-3-aminocyclopentyl]carbamate; tert-Butyl N-[trans-3-aminocyclopentyl]carbamate; tert-butyl n-[(1r,3r)-3-aminocyclopentyl]carbamate; tert-Butyl rac-[(1R,3R)-3-aminocyclopentyl] carbamate; tert-Butyl ((1R,3R)-rel-3-aminocyclopentyl)carbamate; SCHEMBL1013184; PGBVMVTUWHCOHX-HTQZYQBOSA-N; MFCD16037624; MFCD18533495;

Keywords: 1009075-44-8,MFCD16037624,1P0003MM,Carbamic acid, N-[(1R,3R)-3-aminocyclopentyl]-, 1,1-dimethylethyl ester,C10H20N2O2

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Catalog# Purity Size Price Dis. Price Availability Quantity
1P0003MM 95% 100mg $35.00 $26.00 In Stock USA ADD TO CART BUY NOW
1P0003MM 95% 250mg $66.00 $49.00 In Stock USA ADD TO CART BUY NOW
1P0003MM 95% 500mg $116.00 $87.00 In Stock USA ADD TO CART BUY NOW
1P0003MM 95% 1g $186.00 $139.00 In Stock USA ADD TO CART BUY NOW
1P0003MM 95% 5g $587.00 $440.00 In Stock USA ADD TO CART BUY NOW
1P0003MM 95% 10g $951.00 $713.00 In Stock USA ADD TO CART BUY NOW
1P0003MM 95% 25g $1,900.00 $1,425.00 In Stock USA ADD TO CART BUY NOW
1P0003MM 95% 50g $3,165.00 $2,374.00 In Stock USA ADD TO CART BUY NOW

  • Carbamic acid, N-[(1R,3R)-3-aminocyclopentyl]-, 1,1-dimethylethyl ester is a specialized chemical compound that can be used as a building block in the synthesis of various organic molecules. Its structural features, specifically the cyclopentyl ring and the carbamate functional group, make it a valuable intermediate in the design of pharmaceuticals, agrochemicals, and other therapeutic agents.
    
    One key application of this compound in chemical synthesis is in the creation of cyclopeptide or peptidomimetics. The cyclopentyl ring can serve as a conformational constraint within a peptide sequence, thereby inducing a specific secondary structure that could improve the biological activity and stability of the peptide.
    
    Additionally, the amino group can be selectively protected and deprotected, offering a diverse range of functionalization strategies. Such a chiral amino group introduces stereoselectivity, which is crucial in the synthesis of enantiomerically pure substances, a dominant concern in the drug development process.
    
    The carbamate portion of the molecule serves as an amine-protecting group. Upon deprotection, it can yield an amine that can subsequently be used to form amide bonds in peptide coupling reactions or can act as a nucleophile in various other transformations.
    
    Furthermore, the tert-butyl group of the ester aids in purification steps during synthesis due to its ability to be easily detected using chromatographic techniques. Also, because of its relatively high steric bulk, it can be useful in selective reactions where the steric hindrance can prevent unwanted side reactions, thus increasing the yield of the desired product.
    
    In summary, the chemical structure of this carbamic acid ester makes it a versatile intermediate with applications in various synthesis routes where it may add conformational rigidity, stereochemistry, and protection for further chemical transformations, notably in the creation of bioactive molecules.

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