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N-benzoylserine is a compound belonging to the family of organic compounds known as benzoic acids and derivatives. It is derived from the naturally occurring amino acid serine, which is a building block for proteins in the body. N-benzoylserine has a benzoyl group attached to the amino group of serine, making it a derivative of the amino acid. It has been studied for its potential pharmaceutical and biological applications, particularly in drug design and development. Its structure allows for modifications to improve its pharmacological properties, and researchers are interested in exploring its therapeutic potential in treating various diseases and conditions.

4582-71-2

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4582-71-2 Usage

Uses

Used in Pharmaceutical Industry:
N-benzoylserine is used as a building block for the development of new drugs due to its potential biological activities and the ability to modify its structure to improve pharmacological properties.
Used in Drug Design and Development:
N-benzoylserine is used as a starting material for designing and developing new pharmaceutical compounds, as its structure can be modified to enhance its therapeutic potential and treat various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 4582-71-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,8 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4582-71:
(6*4)+(5*5)+(4*8)+(3*2)+(2*7)+(1*1)=102
102 % 10 = 2
So 4582-71-2 is a valid CAS Registry Number.

4582-71-2Relevant academic research and scientific papers

Reactivity of Tyrosyl–Proline toward Benzoylation in Aqueous 1,4-Dioxane

Khachatryan, D. S.,Kochetova, L. B.,Kustova, T. P.,Lokteva, I. I.

, p. 1034 - 1040 (2020/07/25)

Abstract: The kinetics of the reaction of L-tyrosyl-L-proline (Tyr–Pro) with di- andtrinitrophenyl benzoates in aqueous 1,4-dioxane (40 wt percent of water) were studiedin the temperature range 298–313 K. The reaction rate constant k298 was fou

Reactivity of α-Amino Acids in the Reaction with Esters in Aqueous–1,4-Dioxane Media

Kochetova,Kustova,Kuritsyn

, p. 80 - 85 (2018/03/09)

The kinetics of the reaction of a series of α-amino acids with 4-nitrophenyl acetate, 4-nitrophenyl benzoate, and 2,4,6-trinitrophenyl benzoate in aqueous 1,4-dioxane medium has been studied. Kinetics of the reactions involving 4-nitrophenyl acetate and 2,4,6-trinitrophenyl benzoate has complied with the Br?nsted dependence and revealed linear correlation between rate constant logarithm and the energy difference of the frontier orbitals of α-amino acids anions.

PREVENTING OR AMELIORATING AGENT FOR PIGMENTATION

-

, (2012/10/18)

An object is to provide an external preparation for skin preferably usable to prevent or ameliorate pigmentation. The object is achieved by providing a preventing or ameliorating agent for pigmentation, consisting of a compound represented by the following general formula (1), an isomer thereof, and/or a pharmacologically acceptable salt thereof, and an external preparation for skin containing the same as a component: [wherein R1 represents an unsubstituted aromatic group or an aromatic group having any substituent; R2 represents a hydrogen atom, a linear chain or branched chain alkyl group having a number of carbon atom or atoms of 1 to 4, or an acyl group having a linear or branched alkyl chain having a number of carbon atom or atoms of 1 to 4; and R3 represents a hydrogen atom or a linear chain or branched chain alkyl group having a number of carbon atom or atoms of 1 to 4.]

Reactivity of the Amino Groups of α-Amino Acids and Dipeptides in Reaction with Benzoyl Chloride in a Dioxane-Water Solvent

Kuritsyn, L. V.,Kalinina, N. V.

, p. 767 - 770 (2007/10/02)

The kinetic characteristics (rate constants, activation energies, and entropies of activation) for the reaction of a series of α-amino acids and dipeptides with benzoyl chloride in aqueous dioxane are presented.The amino group in the investigated α-amino acids has high reactivity 4 liter/mole*sec>; the dipeptides have lower reactivity 3 liter/mole*sec>.

Catalytic Asymmetric Construction of Morpholines and Piperazines by Palladium-Catalyzed Tandem Allylic Substitution Reactions

Uozumi, Yasuhiro,Tanahashi, Asako,Hayashi, Tamio

, p. 6826 - 6832 (2007/10/02)

Reaction of 1,4-diacetoxy-cis-2-butene (1a) with 2-(benzylamino)ethanol (2a) was catalyzed by a palladium complex (5 mol percent) coordinated with (R)-2,2'-bis(diphenylphosphino)-1,1'-binaphthyl to give optically active (R)-4-benzyl-2-vinylmorpholine (3a)

Composition containing a penem or carbapenem antibiotic and the use of the same

-

, (2008/06/13)

Administration of an N-acylated amino acid in association with a penem or carbapenem antibiotic relieves or eliminates the renal problems associated with administration of the antibiotic alone. The amino acid derivative and antibiotic may be formulated together as a composition or administered separately, either simultaneously or sequentially.

Composition containing a penem or carbapenem antibiotic

-

, (2008/06/13)

Administration of an N-acylated amino acid in association with a penem or carbapenem antibiotic relieves or eliminates the renal problems associated with administration of the antibiotic alone. The amino acid derivative and antibiotic may be formulated together as a composition or administered separately, either simultaneously or sequentially. The composition may be prepared by simple mixing.

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