18926-49-3 Usage
Description
[(2-METHYLBENZYL)THIO]ACETIC ACID, also known as 2-methylbenzylthioacetic acid, is a chemical compound with the molecular formula C9H10O2S. It is a thioether derivative of acetic acid and belongs to the class of benzyl compounds. This versatile compound exhibits a range of biological activities, including analgesic and anti-inflammatory properties, making it a promising candidate for drug discovery and development.
Uses
Used in Pharmaceutical Research:
[(2-METHYLBENZYL)THIO]ACETIC ACID is used as a building block in the production of various drugs and pharmaceutical intermediates, contributing to the development of new medications for various health conditions.
Used in Organic Synthesis:
[(2-METHYLBENZYL)THIO]ACETIC ACID serves as a key component in the synthesis of complex organic molecules, which can be utilized in a wide range of applications, from pharmaceuticals to specialty chemicals.
Used in the Food Industry:
[(2-METHYLBENZYL)THIO]ACETIC ACID is used as a flavoring agent, enhancing the taste and aroma of various food products.
Used in the Cosmetic Industry:
As a fragrance, [(2-METHYLBENZYL)THIO]ACETIC ACID is employed in the formulation of cosmetics, adding pleasant scents to products and improving the overall sensory experience for consumers.
Check Digit Verification of cas no
The CAS Registry Mumber 18926-49-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,9,2 and 6 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 18926-49:
(7*1)+(6*8)+(5*9)+(4*2)+(3*6)+(2*4)+(1*9)=143
143 % 10 = 3
So 18926-49-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O2S/c1-8-4-2-3-5-9(8)6-13-7-10(11)12/h2-5H,6-7H2,1H3,(H,11,12)
18926-49-3Relevant articles and documents
Synthesis of Cyclic α-Diazo-β-keto Sulfoxides in Batch and Continuous Flow
McCaw, Patrick G.,Buckley, Naomi M.,Eccles, Kevin S.,Lawrence, Simon E.,Maguire, Anita R.,Collins, Stuart G.
, p. 3666 - 3679 (2017/04/11)
Diazo transfer to β-keto sulfoxides to form stable isolable α-diazo-β-keto sulfoxides has been achieved for the first time. Both monocyclic and benzofused ketone derived β-keto sulfoxides were successfully explored as substrates for diazo transfer. Use of continuous flow leads to isolation of the desired compounds in enhanced yields relative to standard batch conditions, with short reaction times, increased safety profile, and potential to scale up.
