49591-20-0 Usage
Uses
Used in Pharmaceutical Industry:
N-TERT-BUTYLBENZENESULFINIMIDOYL CHLORIDE is used as a reagent for the synthesis of sulfinamides, which are important intermediates in the development of pharmaceutical compounds. Its ability to react with nucleophiles makes it a key component in creating new drug molecules.
Used in Agrochemical Industry:
In the agrochemical sector, N-TERT-BUTYLBENZENESULFINIMIDOYL CHLORIDE is utilized as a precursor in the production of agrochemicals. Its role in forming sulfinamides contributes to the development of new pesticides and other agricultural chemicals.
Used in Organic Synthesis:
N-TERT-BUTYLBENZENESULFINIMIDOYL CHLORIDE is used as a building block in organic chemistry for the synthesis of a variety of sulfur-containing compounds. Its versatility in reacting with different nucleophiles allows for the creation of a wide range of organic molecules.
Used in Research Applications:
In research settings, N-TERT-BUTYLBENZENESULFINIMIDOYL CHLORIDE is employed as a reagent to explore new chemical reactions and pathways. Its reactivity and ability to form sulfinamides make it an essential tool for advancing scientific knowledge in organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 49591-20-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,5,9 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 49591-20:
(7*4)+(6*9)+(5*5)+(4*9)+(3*1)+(2*2)+(1*0)=150
150 % 10 = 0
So 49591-20-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H14ClNS/c1-10(2,3)12-13(11)9-7-5-4-6-8-9/h4-8H,1-3H3
49591-20-0Relevant academic research and scientific papers
A new method for oxidation of various alcohols to the corresponding carbonyl compounds by using n-t-butylbenzenesulfinimidoyl chloride
Matsuo, Jun-Ichi,Iida, Daisuke,Tatani, Kazuya,Mukaiyama, Teruaki
, p. 223 - 234 (2007/10/03)
Various primary and secondary alcohols were smoothly oxidized to the corresponding aldehydes and ketones by using a new oxidizing agent, N-t-butylbenzenesulfinimidoyl chloride (4a), in the coexistence of DBU or zinc oxide. The present oxidation proceeded under mild conditions via five-membered intramolecular proton-transfer of an alkyl arenesulfinimidate intermediate.
