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16189-10-9

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16189-10-9 Usage

General Description

2-ACETOXYCINNAMIC ACID, also known as O-Acetylsalicylic acid, is a chemical compound with the molecular formula C11H10O4. It is an ester of salicylic acid and acetic acid, and is commonly used as a precursor in the synthesis of various pharmaceutical compounds. 2-ACETOXYCINNAMIC ACID has been found to exhibit anti-inflammatory and analgesic properties, and has been studied for its potential use in the treatment of various medical conditions such as arthritis and cardiovascular disease. Additionally, 2-ACETOXYCINNAMIC ACID has also been investigated for its potential use in the field of organic chemistry as a building block for the synthesis of various organic compounds. Overall, this chemical compound has shown promise in the fields of medicine and organic chemistry for its potential therapeutic and synthetic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 16189-10-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,1,8 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 16189-10:
(7*1)+(6*6)+(5*1)+(4*8)+(3*9)+(2*1)+(1*0)=109
109 % 10 = 9
So 16189-10-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H10O4/c1-8(12)15-10-5-3-2-4-9(10)6-7-11(13)14/h2-7H,1H3,(H,13,14)/b7-6-

16189-10-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-3-(2-acetoxyphenyl)acrylic acid

1.2 Other means of identification

Product number -
Other names azanyl diphenyl phosphate

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:16189-10-9 SDS

16189-10-9Relevant articles and documents

COMPOUNDS AND COMPOSITIONS FOR OCULAR DELIVERY

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Page/Page column 108; 178-179, (2020/05/12)

The present invention provides new prodrags of Sunitinib, Brinzolamide, and Dorzolamide and compositions to treat medical disorders, for example glaucoma, a disorder or abnormality related to an increase in intraocular pressure (TOP), a disorder requiring neuroprotection, age-related macular degeneration, or diabetic retinopathy.

Synthesis of novel 1,2,5-oxadiazoles and evaluation of action against Acinetobacter baumannii

Christoff, Rebecca M.,Murray, Gerald L.,Kostoulias, Xenia P.,Peleg, Anton Y.,Abbott, Belinda M.

supporting information, p. 6267 - 6272 (2017/10/13)

With multidrug resistant bacteria on the rise, novel antibiotics are becoming highly sought after. In 2008, eleven compounds were identified by high throughput screening as inhibitors of BasE, a key enzyme of the non-ribosomal peptide synthetase pathway found in Acinetobacter baumannii. Herein, we describe the preparation of four structurally similar heterocyclic lead compounds from that study, including one 1,2,5-oxadiazole. A further library of 30 analogues containing the oxadiazole moiety was then generated. All compounds were screened against Acinetobacter baumannii and their minimum inhibitory concentration data is reported, with (E)-3-(2-hydroxyphenyl)-N-(4-methyl-1,2,5-oxadiazol-3-yl)acrylamide 32 found to have an MIC of 0.5 mM. This work provides the foundation for further investigation of 1,2,5-oxadizoles as novel inhibitors of A. baumannii.

Novel enzymatic synthesis of 4-O-cinnamoyl quinic and shikimic acid derivatives

Armesto, Nuria,Ferrero, Miguel,Fernandez, Susana,Gotor, Vicente

, p. 5784 - 5787 (2007/10/03)

The first direct synthesis of 4-O-cinnamoyl derivatives of quinic and shikimic acids were accomplished by regioselective esterification with Candida antarctica lipase A. For hydrocinnamic esters, enzymatic transesterification with vinyl esters gave excell

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