18807-67-5 Usage
Description
(2-BenzyloxycarbonylaMino-ethyl)-carbaMic acid benzyl ester is a synthetic compound derived from the reaction of (2-BenzyloxycarbonylaMino-ethyl)-carbaMic acid with benzyl alcohol. It belongs to the family of aminocarbonyl compounds, which are known for their diverse biological activities. The benzyl ester group on the molecule enhances its stability and reduces reactivity, making it easier to handle and store. This chemical holds promising potential for use in pharmaceutical research and development.
Uses
Used in Organic Synthesis:
(2-BenzyloxycarbonylaMino-ethyl)-carbaMic acid benzyl ester is used as a reagent in organic synthesis for its ability to facilitate various chemical reactions and contribute to the formation of complex organic molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (2-BenzyloxycarbonylaMino-ethyl)-carbaMic acid benzyl ester is utilized for its potential applications in the development of new pharmaceuticals. Its unique structure and properties make it a valuable component in the synthesis of bioactive compounds with therapeutic potential.
Used in Pharmaceutical Research and Development:
(2-BenzyloxycarbonylaMino-ethyl)-carbaMic acid benzyl ester is employed in pharmaceutical research and development as a key intermediate in the synthesis of drug candidates. Its stability and reactivity make it suitable for use in the creation of novel therapeutic agents with diverse biological activities.
Check Digit Verification of cas no
The CAS Registry Mumber 18807-67-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,8,0 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 18807-67:
(7*1)+(6*8)+(5*8)+(4*0)+(3*7)+(2*6)+(1*7)=135
135 % 10 = 5
So 18807-67-5 is a valid CAS Registry Number.
18807-67-5Relevant articles and documents
Alkylation of serine at the active site of trypsin.
Lawson,Leafer Jr.,Tewes,Rao
, p. 251 - 262 (1968)
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Doxorubicin immunoconjugates containing bivalent, lysosomally-Cleavable dipeptide linkages
Dubowchik, Gene M,Radia, Shilpa,Mastalerz, Harold,Walker, Michael A.,Firestone, Raymond A.,Dalton King, H.,Hofstead, Sandra J.,Willner, David,Lasch, Shirley J.,Trail, Pamela A.
, p. 1529 - 1532 (2007/10/03)
Bivalent doxorubicin (DOX)-dipeptides (16a-c) were prepared and conjugated to the monoclonal antibody BR96. The dipeptides are cleaved by lysosomal proteases following internalization of the resulting immunoconjugates. Conjugate 18b demonstrated antigen-s
NOVEL UNSYMMETRICAL N,N-BIS(METHYLENE)BIPHOSPHONIC ACIDS OF α,ω-DIAMINES. PREPARATION AND CHARACTERIZATION OF BIS(METHYLENE)>-BIPHOSPHONIC ACID AND BIS(METHYLENE)>-BIPHOSPHONIC ACID
Redmore, Derek,Dhawan, Balram
, p. 233 - 238 (2007/10/02)
Reaction of ethylenediamine with phosphorous acid and formaldehyde in molar ratio 1:2:2 gives bis(methylene)>biphosphonic acid (2a) as the major product.Similarly, reaction of hexamethylenediamine with phosphorous acid and formaldehyde in molar ratio 1:2:2 yields bis(methylene)>biphosphonic acid (2b) which is isolated either as bis(methylene>biphosphonic acid (3b) or as bis(methylene)>biphosphonic acid (4b).Removal of the carbobenzoxy group with HBr 3b or the benzoyl group with HCl from 4b gives pure bis(methylene)>biphosphonic acid (2b).All compounds were characterized by 13C NMR, 31P NMR and elemental analysis.
