70732-64-8 Usage
Derivative of acetic acid
Acetic acid is the parent compound, and 2-[(benzyloxy)carbonyl](ethyl)amino acetic acid is derived from it This means that the compound has a similar structure to acetic acid but with modifications (additions or substitutions) in its structure.
Contains a benzyl group
A phenyl ring (a six-carbon ring with alternating single and double bonds) connected to a methyl group (a single carbon atom with three hydrogen atoms) The benzyl group contributes to the compound's potential pharmacological activity and can influence its properties.
Contains an ethyl group
An ethane molecule with one hydrogen atom replaced by a functional group (in this case, an amino group) The ethyl group may affect the compound's reactivity and its ability to form pharmaceutical compounds.
Contains an amino group
A nitrogen atom bonded to two hydrogen atoms The amino group makes the compound a versatile building block for the synthesis of new compounds and can contribute to its pharmacological activity.
Used as an intermediate in the synthesis of various pharmaceuticals and organic compounds
The compound serves as a starting material or building block in the creation of other compounds This highlights its importance in the field of medicinal chemistry and organic synthesis.
Potential applications in the field of medicinal chemistry
The compound has the potential to be used in the development of drugs for various diseases This indicates that the compound has promise for therapeutic use and further research.
Development of drugs for various diseases
The compound may be used to create medications that target a range of medical conditions This suggests that the compound has a broad scope of potential applications in the pharmaceutical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 70732-64-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,7,3 and 2 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 70732-64:
(7*7)+(6*0)+(5*7)+(4*3)+(3*2)+(2*6)+(1*4)=118
118 % 10 = 8
So 70732-64-8 is a valid CAS Registry Number.
70732-64-8Relevant academic research and scientific papers
IMIDAZOQUINOLINE-TYPE COMPOUNDS AND USES THEREOF
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Paragraph 0013; 00106; 00117, (2021/10/11)
Provided in the present disclosure are imidazoquinoline-type compounds, methods for their preparation, pharmaceutical compositions thereof and their use, wherein the imidazoquinoline-type compounds, upon local administration, form depots inducing cell mediated immune response while mitigating a systemic proinflammatory immune response.
Polypeptoids from n-substituted glycine n-carboxyanhydrides: Hydrophilic, hydrophobic, and amphiphilic polymers with poisson distribution
Fetsch, Corinna,Grossmann, Arlett,Holz, Lisa,Nawroth, Jonas F.,Luxenhofer, Robert
experimental part, p. 6746 - 6758 (2012/03/10)
Preparation of defined and functional polymers has been one of the hottest topics in polymer science and drug delivery in the recent decade. Also, research on (bio)degradable polymers gains more and more interest, in particular at the interface of these t
Synthesis of N-alkyl-N-methyl amino acids. Scope and limitations of base-induced N-alkylation of Cbz-amino acids
Stodulski, Maciej,Mlynarski, Jacek
, p. 970 - 975 (2008/09/21)
The reaction of N-benzyloxycarbonyl derivatives of aliphatic amino acids with NaH/alkyl iodides gave the corresponding N-Cbz-N-alkyl derivatives in good to high yields. The scope and limitations of this simple N-alkylation reaction were investigated as a convenient and flexible attempt to prepare unsymmetrically N,N-diprotected α-amino acids. The procedure is based on the N-alkylation of N-carbamoyl amino acids, a one-pot deprotection/protection sequence without extensive purification of the products. Protection of the carboxyl function is not required while the starting materials are inexpensive and commercially available.
Acyl derivatives
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, (2008/06/13)
Peptide derivatives provided by the present invention are compounds of the general formula STR1 wherein R1 represents a hydrogen atom or the methyl or hydroxymethyl group or a mono-, di- or trihalomethyl mgroup; R2 represents the cha
