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937-56-4

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937-56-4 Usage

Synthesis Reference(s)

Tetrahedron, 50, p. 10483, 1994 DOI: 10.1016/S0040-4020(01)89588-0

Check Digit Verification of cas no

The CAS Registry Mumber 937-56-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,3 and 7 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 937-56:
(5*9)+(4*3)+(3*7)+(2*5)+(1*6)=94
94 % 10 = 4
So 937-56-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H12OS/c1-8(10)7-11-9-5-3-2-4-6-9/h2-6,8,10H,7H2,1H3

937-56-4Relevant articles and documents

Anodic methoxylation of 2-acyloxy-3,3,3-trifluoropropyl sulfides accompanying with [1,2]-rearrangement of the acyloxy group and anodic cyclization of 2-(t-butoxycarbonyl)oxy-3,3,3-trifluoropropyl sulfide

Isokawa, Motoaki,Sano, Masaru,Kubota, Kiyotaka,Suzuki, Katsutoshi,Inagi, Shinsuke,Fuchigami, Toshio

, p. G121 - G127 (2017/11/17)

Anodic methoxylation of 2-acyloxy-3,3,3-trifluoropropyl sulfides was carried out in methanol containing Et3N-3HF as a supporting electrolyte and mediator using an undivided cell to provide the corresponding α-methoxylated products and unexpecte

" On-water " thiolysis of epoxides promoted by PhSZnBr

Propersi, Simona,Tidei, Caterina,Bagnoli, Luana,Marini, Francesca,Testaferri, Lorenzo,Santi, Claudio

, p. 671 - 676 (2014/01/06)

The synthesis of a new bench-stable and odorless zinc thiolate is here reported. The thiolysis of epoxides effected using this reagent showed a considerable rate acceleration of the reaction when effected in "on-water" conditions. In addition, the reactio

LiOH-catalyzed simple ring opening of epoxides under solvent-free conditions

Azizi, Najmedin,Khajeh-Amiri, Alireza,Ghafuri, Hossein,Bolourtchian, Mohammad

scheme or table, p. 1550 - 1557 (2010/09/06)

LiOH has been found to be a very simple and selective catalyst for the rapid and mild synthesis of β-hydroxy sulfides and β-hydroxyl nitriles by ring opening of epoxides with aromatic, aliphatic, and heterocyclic thiols and trimethylsilyl cyanide at room temperature under solvent free conditions. All the reactions proceeded satisfactorily in short times and afforded the corresponding products in good to excellent yields with high regioselectivity and chemoselectivity under mild reaction conditions. Copyright Taylor & Francis Group, LLC.

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