38054-60-3 Usage
Uses
Used in Organic Chemistry:
5-METHYL-3-(METHYLTHIO)-1,4-DIPHENYL-1H-1,2,4-TRIAZOLIUM IODIDE is used as a catalyst for various organic chemistry reactions due to its stability and solubility in organic solvents, facilitating efficient reaction processes.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 5-METHYL-3-(METHYLTHIO)-1,4-DIPHENYL-1H-1,2,4-TRIAZOLIUM IODIDE is utilized as a component in the development of new drugs, leveraging its unique chemical properties to enhance drug efficacy and delivery.
Used in Materials Science:
5-METHYL-3-(METHYLTHIO)-1,4-DIPHENYL-1H-1,2,4-TRIAZOLIUM IODIDE is employed as a component in the creation of advanced materials, contributing to the development of novel materials with improved properties for various applications.
Used in Battery Technology:
As an electrolyte in batteries, 5-METHYL-3-(METHYLTHIO)-1,4-DIPHENYL-1H-1,2,4-TRIAZOLIUM IODIDE is used to improve the performance and efficiency of energy storage systems, taking advantage of its ionic liquid nature to enhance conductivity and stability.
Check Digit Verification of cas no
The CAS Registry Mumber 38054-60-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,0,5 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 38054-60:
(7*3)+(6*8)+(5*0)+(4*5)+(3*4)+(2*6)+(1*0)=113
113 % 10 = 3
So 38054-60-3 is a valid CAS Registry Number.
InChI:InChI=1/C16H16N3S.HI/c1-13-18(14-9-5-3-6-10-14)16(20-2)17-19(13)15-11-7-4-8-12-15;/h3-12H,1-2H3;1H/q+1;/p-1
38054-60-3Relevant academic research and scientific papers
THE CHAIN LENGTHENING OF ALIPHATIC ALDEHYDES WITH THE AID OF "NUCLEOPHILIC CARBENE"
Doleschall, Gabor
, p. 4183 - 4186 (2007/10/02)
The addition of "nucleophilic carbene" on 1,2,4-triazole bases (2) and aldehydes is decisively influenced by the anion present. 5-(α-Hydroxyalkyl)-1,2,4-triazolium chlorides, formed in the addition reaction of 3-methylthio-1,4-diphenyl-1,2,4-triazolium chloride (1c) with aldehydes, can be easily reduced to 5-alkyl-1,2,4-triazolium iodides (5).Reduction of these with NaBH4 affords aldehydes by acidic hydrolysis or carboxylic acids by alkaline hydrolysis, the carbon chain of which has been lengthened by one CH2 group, as compared to the starting aldehyde.
