257938-67-3 Usage
General Description
Boc-4-(4-Hydroxyphenyl)-(3s,4s)-3-Piperidinol is a complex chemical compound. Protecting the amine functionalities during organic synthesis and peptide bond formation can be achieved with the use of Boc-4-(4-Hydroxyphenyl)-(3s,4s)-3-Piperidinol. The Boc (tert-butyloxycarbonyl) group plays a significant role by obstructing the reactive amine group of the molecule, thereby serving as an effective blocking agent. Additionally, the hydroxyphenyl group, effectively influences the chemical properties of the compound and can enhance its reactivity under various conditions. The 3-piperidinol portion of the molecule can participate in numerous biological interactions, offering potential pharmaceutical benefits. However, specific applications and properties will depend on the exact synthesis and chemical environment of this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 257938-67-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,7,9,3 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 257938-67:
(8*2)+(7*5)+(6*7)+(5*9)+(4*3)+(3*8)+(2*6)+(1*7)=193
193 % 10 = 3
So 257938-67-3 is a valid CAS Registry Number.
257938-67-3Relevant articles and documents
Selective NR2B Antagonists
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Paragraph 0366, (2015/07/15)
The disclosure generally relates to compounds of formula I, including their salts, as well as compositions and methods of using the compounds. The compounds are ligands of the NR2B receptor and may be useful for the treatment of various disorders of the c
Piperidine renin inhibitors: from leads to drug candidates
Maerki, H. P.,Binggeli, A.,Bittner, B.,Bohner-Lang, V.,Breu, V.,Bur, D.,Coassolo, Ph.,Clozel, J. P.,D'Arcy, A.,Doebeli, H.,Fischli, W.,et al.
, p. 21 - 28 (2007/10/03)
Non-peptidomimetic renin inhibitors of the piperidine type represent a novel structural class of compounds potentially free of the drawbacks seen with peptidomimetic compounds so far. Synthetic optimization in two structural series focusing on improvement
Solid-phase synthesis of aspartic peptidase inhibitors: 3-alkoxy-4-aryl piperidines.
Bursavich,Rich
, p. 2625 - 2628 (2007/10/03)
[reaction: see text]. The 3-alkoxy-4-aryl piperidines are non-peptide peptidomimetic inhibitors of several aspartic peptidases. The solid-phase functionalization of 3,4-disubstituted piperidine scaffolds using a traceless linker strategy is described. Syn