58511-20-9 Usage
General Description
(4-Methylbenzyl)thio]acetic acid is a chemical compound with the molecular formula C10H12OS and is also known as 4-methylbenzylthioacetic acid. It has a molecular weight of 188.27 g/mol. (4-METHYLBENZYL)THIO]ACETIC ACID is a thiol derivative and contains a benzyl group attached to a thioacetic acid moiety. It is commonly used in the synthesis of organic compounds and pharmaceuticals. The compound may also have potential applications in the field of medicinal chemistry and drug research due to its structural characteristics and properties. Additionally, it may have industrial uses in the production of certain chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 58511-20-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,5,1 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 58511-20:
(7*5)+(6*8)+(5*5)+(4*1)+(3*1)+(2*2)+(1*0)=119
119 % 10 = 9
So 58511-20-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O2S/c1-8-2-4-9(5-3-8)6-13-7-10(11)12/h2-5H,6-7H2,1H3,(H,11,12)
58511-20-9Relevant articles and documents
Benzylthioacetamide compounds and preparation method and application thereof
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Paragraph 0047-0050, (2020/06/16)
The invention belongs to the technical field of plant growth regulators, and particularly discloses a benzylthioacetamide compound and a preparation method and application thereof. The structure of the compound is as shown in a formula I which is describe
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.
