15570-12-4 Usage
Description
3-Methoxybenzenethiol, also known as 3-Methoxythiophenol, is an organic compound with the chemical formula C7H8OS. It is a clear colorless to light yellow liquid and is a labeled analogue of phencyclidine, differing in terms of binding affinity.
Uses
Used in Pharmaceutical Industry:
3-Methoxybenzenethiol is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure and properties make it a valuable building block in the development of new drugs.
Used in Chemical Synthesis:
3-Methoxythiophenol is used in the preparation of allenes, which are important intermediates in organic chemistry. Allenes have a wide range of applications, including the synthesis of complex organic molecules and the development of new materials.
Used in Research and Development:
Due to its unique chemical properties and potential applications, 3-Methoxybenzenethiol is also used in research and development for exploring new reactions, understanding its reactivity, and identifying novel applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 15570-12-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,5,7 and 0 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 15570-12:
(7*1)+(6*5)+(5*5)+(4*7)+(3*0)+(2*1)+(1*2)=94
94 % 10 = 4
So 15570-12-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H8OS/c1-8-6-3-2-4-7(9)5-6/h2-5,9H,1H3/p-1
15570-12-4Relevant articles and documents
Crampton
, p. 2112 (1971)
Copper-Catalyzed Direct Synthesis of Aryl Thiols from Aryl Iodides Using Sodium Sulfide Aided by Catalytic 1,2-Ethanedithiol
Xue, Hongyu,Jing, Bing,Liu, Shasha,Chae, Junghyun,Liu, Yajun
, p. 2272 - 2276 (2017/10/06)
A copper-catalyzed direct and effective synthesis of aryl thiols from aryl iodides using readily available Na 2 S·9H 2 O and 1,2-ethanedithiol was described. A variety of aryl thiols were readily obtained in yields of 76-99%. In this protocol, Na 2 S·9H 2 O was used as ultimate sulfur source, and 1,2-ethanedithiol functioned as an indispensable catalytic reagent.
Scandium triflate-catalyzed one-pot domino approach towards general and efficient syntheses of unsymmetrical 9-substituted xanthene derivatives
Singh, Ritesh,Panda, Gautam
scheme or table, p. 1097 - 1105 (2010/06/15)
A general and efficient one-pot cascade/tandem approach to synthesize unsymmetrical 9-aryl/heteroaryl xanthenes has been developed under extremely mild reaction conditions using 10 mol% Sc(OTf)3 as a catalyst. This strategy has been further extended to synthesize 9-(thioaryl) xanthenes through tandem carbon-sulfur (C-S) and carbon-carbon (C-C) bond formation. Novel C-C and C-S bond cleavage promoted by Sc(OTf)3 is also discussed during mechanistic investigation. The Royal Society of Chemistry.