54744-70-6 Usage
Uses
Used in Pharmaceutical Research and Development:
A-(Benzylthio)acetamide serves as a valuable intermediate in the development of new drugs for a variety of diseases and conditions. Its unique structure and properties contribute to its potential as a key component in medicinal chemistry.
Used in Organic Synthesis:
In the field of organic synthesis, A-(Benzylthio)acetamide is employed as a versatile intermediate for the production of other organic compounds. Its ability to be utilized in the creation of various chemical products highlights its importance in synthetic chemistry.
Used in Chemical Product Creation:
A-(Benzylthio)acetamide is also recognized for its role in the creation of different chemical products, further emphasizing its value in the chemical industry and research.
Check Digit Verification of cas no
The CAS Registry Mumber 54744-70-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,7,4 and 4 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 54744-70:
(7*5)+(6*4)+(5*7)+(4*4)+(3*4)+(2*7)+(1*0)=136
136 % 10 = 6
So 54744-70-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H11NOS/c10-9(11)7-12-6-8-4-2-1-3-5-8/h1-5H,6-7H2,(H2,10,11)
54744-70-6Relevant academic research and scientific papers
Mass Spectrometry of 2-Alkylthio-2-methylpropanoic Acids and Their Esters and Amides. Structural and Steric Effects on the McLafferty Rearrangement
Mori, Yuji,Fujiwara, Shigeru,Miyachi, Toshiko,Kitanishi, Hiroyuki,Oya, Masayuki,et al.
, p. 1505 - 1517 (2007/10/02)
The electron ionization mass spectra (MS) of S-methylated derivatives of N-(2-mercapto-2-methylpropanoyl)-L-cysteine and 2-alkylthio-2-methylpropanoic acids, as well as their esters and amides, were examined.Use of the deuterium labeling technique and accurate mass measurement supported the proposed fragmentation pathways.Extensive loss of CH2S from a molecular ion by the McLafferty rearrangementof a primary hydrogen is important in the MS of S-methyl compounds of amide derivatives.It was demonstrated that the intensity of the rearrangement ion decreases in the order of amide, ester, and acid, and in the case if amides the reaarangement is suppressed by the nonbonded interaction between methyl groups on the α carbon and the amide nitrogen.Keywords-N-(2-mercapto-2-methylpropanoyl)-L-cysteine; 2-alkylthio-2-methylpropanoic acid and methyl ester; 2-alkylthio-2-methylpropanamide; electron impact mass spectrometry; McLafferty rearrangement; steric interaction
