Welcome to LookChem.com Sign In|Join Free

CAS

  • or
(3-CHLORO-BENZOYLAMINO)-ACETIC ACID is an organic compound with the molecular structure featuring a chloro-benzoyl group and an amino group attached to an acetic acid backbone. It is characterized by its potential pharmaceutical and chemical applications due to its unique molecular structure and functional groups.

57728-59-3 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 57728-59-3 Structure
  • Basic information

    1. Product Name: (3-CHLORO-BENZOYLAMINO)-ACETIC ACID
    2. Synonyms: 2-[(3-CHLOROBENZOYL)AMINO]ACETIC ACID;(3-CHLORO-BENZOYLAMINO)-ACETIC ACID;TIMTEC-BB SBB004570;m-Chlorohippuric acid
    3. CAS NO:57728-59-3
    4. Molecular Formula: C9H8ClNO3
    5. Molecular Weight: 213.62
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 57728-59-3.mol
  • Chemical Properties

    1. Melting Point: 144-147°C
    2. Boiling Point: 440.5°C at 760 mmHg
    3. Flash Point: 220.2°C
    4. Appearance: /
    5. Density: N/A
    6. Vapor Pressure: 1.55E-08mmHg at 25°C
    7. Refractive Index: N/A
    8. Storage Temp.: Refrigerator
    9. Solubility: DMSO (Slightly), Methanol (Slightly)
    10. CAS DataBase Reference: (3-CHLORO-BENZOYLAMINO)-ACETIC ACID(CAS DataBase Reference)
    11. NIST Chemistry Reference: (3-CHLORO-BENZOYLAMINO)-ACETIC ACID(57728-59-3)
    12. EPA Substance Registry System: (3-CHLORO-BENZOYLAMINO)-ACETIC ACID(57728-59-3)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 57728-59-3(Hazardous Substances Data)

57728-59-3 Usage

Uses

Used in Pharmaceutical Industry:
(3-CHLORO-BENZOYLAMINO)-ACETIC ACID is used as an intermediate compound for the synthesis of various pharmaceuticals, particularly those with anticonvulsant and cardiotonic properties. Its molecular structure allows for further chemical modifications to enhance its therapeutic effects and target specific medical conditions.
Used in Chemical Research:
In the field of chemical research, (3-CHLORO-BENZOYLAMINO)-ACETIC ACID serves as a valuable compound for studying the effects of chloro and amino substitutions on the chemical and biological properties of acetic acid derivatives. This can lead to the development of new compounds with improved characteristics and applications.
Used in Drug Metabolism Studies:
(3-CHLORO-BENZOYLAMINO)-ACETIC ACID, being a metabolite of certain drugs, is used in drug metabolism studies to understand the biotransformation processes in the body. This knowledge can be applied to optimize drug dosages, reduce side effects, and improve the overall efficacy of medications.

Check Digit Verification of cas no

The CAS Registry Mumber 57728-59-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,7,2 and 8 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 57728-59:
(7*5)+(6*7)+(5*7)+(4*2)+(3*8)+(2*5)+(1*9)=163
163 % 10 = 3
So 57728-59-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H8ClNO3/c10-7-3-1-2-6(4-7)9(14)11-5-8(12)13/h1-4H,5H2,(H,11,14)(H,12,13)/p-1

57728-59-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(3-chlorobenzoyl)amino]acetic acid

1.2 Other means of identification

Product number -
Other names 3-chlorobenzoylglycine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:57728-59-3 SDS

57728-59-3Relevant articles and documents

MAGL inhibitor as well as preparation method and application thereof

-

, (2021/03/30)

The invention relates to a compound shown as a formula I in the description and a pharmaceutically acceptable salt thereof, a preparation method, an intermediate for preparing the compound, a composition containing the compound or salt, and application of

Synthesis and evaluation of new phenyl acrylamide derivatives as potent non-nucleoside anti-HBV agents

Gu, Xiaoke,Zhang, Yinpeng,Zou, Yueting,Li, Xin,Guan, Mingyu,Zhou, Qingqing,Qiu, Jingying

, (2020/12/09)

As a continuation of our previous work, a series of new phenyl acrylamide derivatives (4Aa-g, 4Ba-t, 5 and 6a-c) were designed and synthesized as non-nucleoside anti-HBV agents. Among them, compound 4Bs could potently inhibit HBV DNA replication in wild-type and lamivudine (3TC)/entecavir resistant HBV mutant strains with IC50 values of 0.19 and 0.18 μM, respectively. Notably, the selective index value of 4Bs was above 526, indicating the favorable safety profile. Interestingly, unlike nucleoside analogue 3TC, 4Bs could significantly inhibit 3.5 kb pgRNA expression. Molecular docking study revealed that 4Bs could fit well into the dimer-dimer interface of HBV core protein by hydrophobic, π–π and H-bond interactions. Considering the potent anti-HBV activity, low toxicity and diverse anti-HBV mechanism from that of nucleoside anti-HBV agent 3TC, compound 4Bs might be a promising lead to develop novel non-nucleoside anti-HBV therapeutic agents, and warranted further investigation.

Substituted [1,2,4]triazolo[4,3-a]pyrazines as antidiabetics

-

Page/Page column 15, (2021/01/26)

Compounds for the treatment of hyperglycemia and/or diabetes are provided. The compounds, which inhibit the enzyme dipeptidyl peptidase (DPP-4), are based on the structure where n1=0-2 such as 0 or 1; R1 is i) a saturated or unsaturated, substituted or un

4-Sulfamoylphenylalkylamides as Inhibitors of Carbonic Anhydrases Expressed in Vibrio cholerae

Mancuso, Francesca,De Luca, Laura,Bucolo, Federica,Vrabel, Milan,Angeli, Andrea,Capasso, Clemente,Supuran, Claudiu T.,Gitto, Rosaria

, p. 3787 - 3794 (2021/10/20)

A current issue of antimicrobial therapy is the resistance to treatment with worldwide consequences. Thus, the identification of innovative targets is an intriguing challenge in the drug and development process aimed at newer antimicrobial agents. The state-of-art of anticholera therapy might comprise the reduction of the expression of cholera toxin, which could be reached through the inhibition of carbonic anhydrases expressed in Vibrio cholerae (VchCAα, VchCAβ, and VchCAγ). Therefore, we focused our interest on the exploitation of sulfonamides as VchCA inhibitors. We planned to design and synthesize new benzenesulfonamides based on our knowledge of the VchCA catalytic site. The synthesized compounds were tested thus collecting useful SAR information. From our investigation, we identified new potent VchCA inhibitors, some of them displayed high affinity toward VchCAγ class, for which few inhibitors are currently reported in literature. The best interesting VchCAγ inhibitor (S)-N-(1-oxo-1-((4-sulfamoylbenzyl)amino)propan-2-yl)furan-2-carboxamide (40) resulted more active and selective inhibitor when compared with acetazolamide (AAZ) as well as previously reported VchCA inhibitors.

MAGL inhibitor and preparation method and application thereof

-

Paragraph 0011-0013, (2020/08/30)

The invention belongs to the field of medicines, and relates to a compound and a pharmaceutically acceptable salt thereof, a preparation method thereof, a composition containing the compound or the salt, and their use in the treatment of MAGL-mediated dis

A convenient method for synthesis of 5-chloro-2-aryloxazole-4-carbaldehyde with vilsmeier reagent

Jin, Can,Chen, Jun,Su, Weike

experimental part, p. 153 - 161 (2011/04/21)

A convenient method for synthesis of 5-chloro-2-aryloxazole-4-carbaldehyde 3 in moderate to good yields had been developed via the Vilsmeier reaction of readily available N-arylglycine 2 at 100 °C, provided a novel route for the construction of nitrogen heterocycles. A series of these compounds were synthesized by this method and optimization of conditions was performed. The Japan Institute of Heterocyclic Chemistry.

Structure-Reactivity Studies on the Equilibrium Reaction between Phenolate Ions and 2-Aryloxazolin-5-ones: Data Consistent with a Concerted Acyl-Group-Transfer Mechanism

Curran, Terence C,Farrar, Charles R.,Niazy, Omima,Williams, Andrew

, p. 6828 - 6837 (2007/10/02)

The rate and equilibrium constants for the reaction between phenolate anions and 2-aryloxazolin-5-ones have been measured as a function of the structures Ar and Ar'.The change in "effective" charge on both phenol-leaving oxygen and endocyclic oxygen from ground to transition state, as determined from the relevant Broensted parameters, is substantial and essentially additive consistent with a concerted displacement mechanism.The stepwise mechanism requires a small change in effective charge on the phenol oxygen because departure of phenolate ion from the tetrahedral intermediate cannot be rate limiting.Hydroxide ion attack on the C-5 atom of the oxazolinone to yield a benzoylglycine has a Hammett ?- dependence which can only arise from a concerted displacement; the rate-limiting step for the stepwise mechanism is the addition of hydroxide and the transition state of the rate-limiting step will therefore not involve much endocyclic C-O bond fission.An inverse deuterium oxide solvent isotope effect indicates that the observed general-acid catalysis has a specific-acid/nucleophilic mechanism; both hydroxide and oxonium ion catalysis are demonstrated by using 18O-labeling experiments to involve nucleophilic attack at the carbonyl (C-5) center.The equilibrium constant for reaction of azide ion with 2-phenyloxazolin-5-ones has been measured; it is suggested that the absence of racemization during azide coupling in peptide synthesis is related to the very unfavorable equilibrium constant for oxazolinone formation compared with that of activated oxygen esters.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 57728-59-3
  • ©2008 LookChem.com,License:ICP NO.:Zhejiang16009103 complaints:service@lookchem.com
  • [Hangzhou]86-0571-87562588,87562578,87562573 Our Legal adviser: Lawyer