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5180-75-6

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5180-75-6 Usage

General Description

4-[(ETHOXYCARBONYL)AMINO]BENZOIC ACID is a chemical compound with the molecular formula C11H13NO5. It is a derivative of benzoic acid and contains an ethoxycarbonylamine functional group. 4-[(ETHOXYCARBONYL)AMINO]BENZOIC ACID is commonly used in pharmaceutical and medical research due to its potential therapeutic properties. It is also utilized in organic synthesis and as a starting material for the production of various pharmaceuticals. Additionally, 4-[(ETHOXYCARBONYL)AMINO]BENZOIC ACID has been studied for its anti-inflammatory and analgesic effects, making it a valuable tool in the development of new drugs and treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 5180-75-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,8 and 0 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5180-75:
(6*5)+(5*1)+(4*8)+(3*0)+(2*7)+(1*5)=86
86 % 10 = 6
So 5180-75-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H11NO4/c1-2-15-10(14)11-8-5-3-7(4-6-8)9(12)13/h3-6H,2H2,1H3,(H,11,14)(H,12,13)

5180-75-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-((Ethoxycarbonyl)amino)benzoic acid

1.2 Other means of identification

Product number -
Other names 4-ethoxycarbonylamino-benzoic acid

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:5180-75-6 SDS

5180-75-6Relevant articles and documents

Design and development of novel p-aminobenzoic acid derivatives as potential cholinesterase inhibitors for the treatment of Alzheimer's disease

Shrivastava, Sushant K.,Sinha, Saurabh K.,Srivastava, Pavan,Tripathi, Prabhash N.,Sharma, Piyoosh,Tripathi, Manish K.,Tripathi, Avanish,Choubey, Priyanka K.,Waiker, Digambar K.,Aggarwal, Lalit M.,Dixit, Manish,Kheruka, Subhash C.,Gambhir, Sanjay,Shankar, Sharmila,Srivastava, Rakesh K.

, p. 211 - 223 (2019)

Based on the quantitative structure-activity relationship (QSAR), some novel p-aminobenzoic acid derivatives as promising cholinesterase enzyme inhibitors were designed, synthesized, characterized and evaluated to enhance learning and memory. The in vitro

Synthesis, analysis, cholinesterase-inhibiting activity and molecular modelling studies of 3-(dialkylamino)-2-hydroxypropyl 4-[(alkoxy-carbonyl)amino]benzoates and their quaternary ammonium salts

Padrtova, Tereza,Marvanova, Pavlina,Odehnalova, Klara,Kubinova, Renata,Parravicini, Oscar,Garro, Adriana,Enriz, Ricardo D.,Humpa, Otakar,Oravec, Michal,Mokry, Petr

, (2017/12/05)

Tertiary amines 3-(dialkylamino)-2-hydroxypropyl 4-[(alkoxycarbonyl)amino]benzoates and their quaternary ammonium salts were synthesized. The final step of synthesis of quaternary ammonium salts was carried out by microwave-assisted synthesis. Software-ca

Oxime-Based carbonates as useful reagents for both n-protection and peptide coupling

Jad, Yahya El-Sayed,Khattab, Sherine N.,El-Faham, Ayman,Albericio, Fernando

, p. 14361 - 14376 (2013/03/13)

We have demonstrated that oxime-based mixed carbonates are very effective reagents for both N-protection and peptide coupling.

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