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10-Butylphenothiazine 5,5-dioxide, also known as 10-butyl-10H-phenothiazine-5,5-dioxide, is a chemical compound with the molecular formula C14H15NOS. It is a derivative of phenothiazine, a heterocyclic compound with a tricyclic structure consisting of two benzene rings and a thiazine ring. This specific compound features a butyl group attached to the 10th position of the phenothiazine core, and the 5,5-dioxide functional group indicates the presence of an additional oxygen atom in the thiazine ring, forming a dioxide. 10-Butylphenothiazine 5,5-dioxide is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly those with antipsychotic, antiemetic, and sedative properties. Its chemical structure and properties make it a versatile building block in the development of new therapeutic agents.

6109-15-5

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6109-15-5 Usage

Chemical class

Phenothiazine

Composition

Butyl group attached to the phenothiazine core, dioxide group at the 5,5-positions

Applications

Pharmacology and medicine

Antipsychotic effects

Blocks dopamine receptors in the brain

Antiemetic properties

Useful in treating nausea and vomiting

Potential

Inhibiting the growth of cancer cells

Versatility

Various pharmaceutical and medical applications

Check Digit Verification of cas no

The CAS Registry Mumber 6109-15-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,0 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6109-15:
(6*6)+(5*1)+(4*0)+(3*9)+(2*1)+(1*5)=75
75 % 10 = 5
So 6109-15-5 is a valid CAS Registry Number.

6109-15-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 10-Butyl-10H-phenothiazine 5,5-dioxide

1.2 Other means of identification

Product number -
Other names 10-butyl-10H-phenothiazine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6109-15-5 SDS

6109-15-5Downstream Products

6109-15-5Relevant academic research and scientific papers

Sodium sulfate-hydrogen peroxide-sodium chloride adduct: selective protocol for the oxidative bromination, iodination and temperature dependent oxidation of sulfides to sulfoxides and sulfones

Gayakwad, Eknath M.,Patel, Khushbu P.,Shankarling, Ganapati S.

supporting information, p. 6001 - 6009 (2019/04/17)

The regioselective bromination and iodination of unprotected aromatic primary amines using enclathrated hydrogen peroxide as an oxidant under mild conditions has been developed, in which potassium bromide (KBr) and potassium iodide (KI) were used as brominating and iodinating agents, respectively. The adduct shows not only regioselectivity for para- or ortho-isomers but also a remarkable chemoselectivity for monobromination. Selective oxidation of sulfides to sulfoxides and sulfones has also been studied and good to excellent yields of the desired products were obtained. Acetic acid was found to be the solvent of choice for these reactions. This simple method represents an ecologically benign and alternative pathway for the oxidative halogenation of anilines and the oxidation of sulfides to sulfoxides and sulfones.

Nonanebis(peroxoic acid) mediated efficient and selective oxidation of sulfide

Gayakwad, Eknath M.,Patil, Vilas V.,Shankarling, Ganapati S.

, p. 223 - 230 (2016/01/12)

Two efficient and rapid protocols for the selective oxidation of sulfide in the presence of various oxidizable functionalities such as -CHO, -CH2-OH, alkene and tert amine were investigated, using nonanebis(peroxoic acid) as an oxidant. The acetonitrile based system offers selective oxidation to sulfoxide and sulfone, while the water based system gives selective sulfone formation with a high conversion and 90-100% selectivity. Recovery and recycling of the parent acid of up to 75-80% was achieved in the water based protocol.

Selective oxidaton methods for preparation of N-alkylphenothiazine sulfoxides and sulfones

Tosa, Monica,Paizs, Csaba,Majdik, Cornelia,Poppe, Laszlo,Kolonits, Pal,Silberg, Ioan A.,Novak, Lajos,Irimie, Florin-Dan

, p. 277 - 282 (2007/10/03)

Efficient and selective oxidation methods for preparation of N-alkylphenothiazine sulfoxides 2a-h and sulfones 3a-h starting from N-alkylphenothiazines 1a-h are described.

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