Category: 887757-51-9

Kumar, V. Pavan et al. published their research in Tetrahedron Letters in 2006 | CAS: 887757-51-9

Benzyl (3-hydroxypropyl)(methyl)carbamate (cas: 887757-51-9) belongs to amides. Amides include many other important biological compounds, as well as many drugs like paracetamol, penicillin and LSD. Low-molecular-weight amides, such as dimethylformamide, are common solvents. As a result of interactions such as these, the water solubility of amides is greater than that of corresponding hydrocarbons. These hydrogen bonds are also have an important role in the secondary structure of proteins.SDS of cas: 887757-51-9

Aqueous phase mono-protection of amines and amino acids as N-benzyloxycarbonyl derivatives in the presence of β-cyclodextrin was written by Kumar, V. Pavan;Reddy, M. Somi;Narender, M.;Surendra, K.;Nageswar, Y. V. D.;Rao, K. Rama. And the article was included in Tetrahedron Letters in 2006.SDS of cas: 887757-51-9 The following contents are mentioned in the article:

A simple and selective protection of amines/amino acids with Cbz-Cl was achieved in aqueous phase with catalytic amounts of β-cyclodextrin in high yields at room temperature This reaction proceeds without the formation of any byproducts and has advantages over existing methods. This study involved multiple reactions and reactants, such as Benzyl (3-hydroxypropyl)(methyl)carbamate (cas: 887757-51-9SDS of cas: 887757-51-9).

Benzyl (3-hydroxypropyl)(methyl)carbamate (cas: 887757-51-9) belongs to amides. Amides include many other important biological compounds, as well as many drugs like paracetamol, penicillin and LSD. Low-molecular-weight amides, such as dimethylformamide, are common solvents. As a result of interactions such as these, the water solubility of amides is greater than that of corresponding hydrocarbons. These hydrogen bonds are also have an important role in the secondary structure of proteins.SDS of cas: 887757-51-9

Referemce:
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics

Dhingra Verma, Kirti et al. published their research in ChemPlusChem in 2012 | CAS: 887757-51-9

Benzyl (3-hydroxypropyl)(methyl)carbamate (cas: 887757-51-9) belongs to amides. In primary and secondary amides, the presence of N–H dipoles allows amides to function as H-bond donors as well. Thus amides can participate in hydrogen bonding with water and other protic solvents; the oxygen atom can accept hydrogen bonds from water and the N–H hydrogen atoms can donate H-bonds. As a result of interactions such as these, the water solubility of amides is greater than that of corresponding hydrocarbons. These hydrogen bonds are also have an important role in the secondary structure of proteins.Formula: C12H17NO3

Magnetic-Field-Dependent 1H Relaxivity Behavior of Biotin/Avidin-Based Magnetic Resonance Imaging Probes was written by Dhingra Verma, Kirti;Mishra, Anurag;Engelmann, Joern;Beyerlein, Michael;Maier, Martin E.;Logothetis, Nikos K.. And the article was included in ChemPlusChem in 2012.Formula: C12H17NO3 The following contents are mentioned in the article:

One major challenge in noninvasive mapping of various mol. targets is their inherently low in vivo concentration coupled with the insensitivity of imaging modalities, such as the widely used magnetic resonance imaging (MRI). Development of agents with high sensitivity and specificity is of paramount importance for structural and functional noninvasive imaging. The design, synthesis, and physiochem. characterization of two gadolinium-based contrast agents (CAs) for MRI, the sensitivity of which was optimized by exploiting the well-established biotin-avidin amplification strategies, are reported. The relaxivity of these agents showed a large increase if bound to avidin; specifically, the first compound showed an approx. 1000 % increase in transverse proton relaxivity (r2p), whereas the second compound had an approx. 250 % r2p increase. The increase in r2p was magnetic field independent in the range of 1.5-16.4 T whereas the longitudinal proton relaxivity (r1p) showed strong field dependence. The CAs were further characterized by measuring luminescence lifetimes and emission spectral changes upon addition of avidin to their Eu3+ analogs. The difference in relaxation rate behavior of both complexes was explained on the basis of hydration number modulation and the “global/internal motion concept”. The association constant of these CAs with avidin was found to be in the range of approx. 1015 M-1, which shows that the coupling of biotin to Gd-DO3A did not affect its affinity for binding to avidin (DO3A=1,4,7,10-tetraazacyclododecane-1,4,7-triacetic acid). This study involved multiple reactions and reactants, such as Benzyl (3-hydroxypropyl)(methyl)carbamate (cas: 887757-51-9Formula: C12H17NO3).

Benzyl (3-hydroxypropyl)(methyl)carbamate (cas: 887757-51-9) belongs to amides. In primary and secondary amides, the presence of N–H dipoles allows amides to function as H-bond donors as well. Thus amides can participate in hydrogen bonding with water and other protic solvents; the oxygen atom can accept hydrogen bonds from water and the N–H hydrogen atoms can donate H-bonds. As a result of interactions such as these, the water solubility of amides is greater than that of corresponding hydrocarbons. These hydrogen bonds are also have an important role in the secondary structure of proteins.Formula: C12H17NO3

Referemce:
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics