56358-04-4 Usage
General Description
Nonyl(phenyl)sulfane, also known as NP thioether, is a chemical compound composed of a nonyl group (nine carbon atoms) attached to a phenyl group (aromatic ring), both of which are connected to a sulfur atom. It is commonly used as a reagent in organic synthesis and as a sulfur transfer agent in chemical reactions, particularly in the development of pharmaceuticals and agrochemicals. NP thioether is also used in the production of specialty chemicals and industrial materials. It is known for its mild and selective reactivity, making it a valuable tool in the field of organic chemistry. Additionally, it is an important intermediate in the manufacturing of surfactants and other industrial products. Overall, nonyl(phenyl)sulfane plays a crucial role in various chemical processes and applications, contributing to the advancement of science and technology.
Check Digit Verification of cas no
The CAS Registry Mumber 56358-04-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,3,5 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 56358-04:
(7*5)+(6*6)+(5*3)+(4*5)+(3*8)+(2*0)+(1*4)=134
134 % 10 = 4
So 56358-04-4 is a valid CAS Registry Number.
56358-04-4Relevant articles and documents
Odorless diphenyl diselenide and disulfide: Syntheses and applications
Patra, Pranab K.,Shanmugasundaram, Kandasamy,Matoba, Manabu,Nishide, Kiyoharu,Kajimoto, Tetsuya,Node, Manabu
, p. 447 - 457 (2007/10/03)
Bis[4-(trimethylsilyl)phenyl]diselenide (3) and bis[4-(trimethylsilyl) phenyl]disulfide (31) are found to be odorless equivalents of the commonly used diphenyl diselenide and diphenyl disulfide, respectively. The diselenide 3 is shown to be useful in the preparation of odorless selenium(II) chloride 26 and selenium(IV) trichloride 28 that follow similar reactivity patterns to their phenyl derivatives and can be stored refrigerated under dry conditions. The corresponding selenium(II) bromide had to be prepared fresh from 3 before use. It is also shown that the trimethylsilyl group in the sulfide products can be protodesilylated quantitatively using TFA. Georg Thieme Verlag Stuttgart.
