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6-Oxa-3-azabicyclo[3.1.0]hexane, 3-[(4-methylphenyl)sulfonyl]-, with the chemical formula C13H17NO3S, is a white solid organic compound belonging to the sulfonyl class. It has a molecular weight of 263.34 g/mol and is characterized by the presence of a sulfonyl group. 6-Oxa-3-azabicyclo[3.1.0]hexane, 3-[(4-methylphenyl)sulfonyl]serves as a versatile building block and intermediate in the pharmaceutical industry for the synthesis of various drugs and as a reagent in chemical reactions to introduce sulfonyl groups into organic compounds.

159555-66-5

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159555-66-5 Usage

Uses

Used in Pharmaceutical Industry:
6-Oxa-3-azabicyclo[3.1.0]hexane, 3-[(4-methylphenyl)sulfonyl]is used as a building block or intermediate for the synthesis of various pharmaceutical drugs. Its unique structure and sulfonyl group enable the development of new drug candidates with potential therapeutic applications.
Used in Chemical Reactions:
6-Oxa-3-azabicyclo[3.1.0]hexane, 3-[(4-methylphenyl)sulfonyl]is also used as a reagent in chemical reactions to introduce the sulfonyl group into organic compounds. The sulfonyl group can enhance the reactivity and properties of the target molecules, making it a valuable tool in organic synthesis.
Safety Precautions:
It is important to handle 6-Oxa-3-azabicyclo[3.1.0]hexane, 3-[(4-methylphenyl)sulfonyl]with care, as it may have potential hazards and associated safety risks. Proper safety measures should be taken during its storage, handling, and use to minimize any risks to human health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 159555-66-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,5,5 and 5 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 159555-66:
(8*1)+(7*5)+(6*9)+(5*5)+(4*5)+(3*5)+(2*6)+(1*6)=175
175 % 10 = 5
So 159555-66-5 is a valid CAS Registry Number.

159555-66-5Downstream Products

159555-66-5Relevant academic research and scientific papers

The use of vinyl sulfonium salts in the stereo-controlled asymmetric synthesis of epoxide- and aziridine-fused heterocycles: Application to the synthesis of (-)-balanol

Unthank, Matthew G.,Hussain, Nigel,Aggarwal, Varinder K.

, p. 7066 - 7069 (2007/10/03)

(Chemical Equation Presented) Lift your ylides: An asymmetric, epoxy-annulation reaction mediated by a vinyl sulfonium salt converts aminoaldehydes and -ketones into fused heterocyclic epoxides. The methodology was extended to an aziridine-annulation reac

Organolithium-induced synthesis of acyclic unsaturated amino alcohols from epoxides of dihydropyrroles and tetrahydropyridines

Hodgson, David M.,Miles, Timothy J.,Witherington, Jason

, p. 9729 - 9742 (2007/10/03)

The alkylative double ring-opening of Bus-protected 2,5-dihydropyrrole epoxides 13 and 29 with organolithiums to give 3-substituted 1-aminobut-3-en-2-ols 13-19 and 30-32 are described. Bus-protected tetrahydropyridine epoxide 38 reacts with organolithiums to give 4-substituted 1-aminobut-4-en-3-ols 39 and tetrahydropyridinol 40.

Use of 7-(2-oxa-5,8-diazabicyclo[4.3.0]non-8-yl)-quinolone carboxylic acid and naphthyridon carboxylic acid derivatives for the treatment of Helicobacter pylori infections and associated gastroduodenal diseases

-

, (2008/06/13)

PCT No. PCT/EP97/06781 Sec. 371 Date Jun. 14, 1999 Sec. 102(e) Date Jun. 14, 1999 PCT Filed Dec. 4, 1997 PCT Pub. No. WO98/26779 PCT Pub. Date Jun. 25, 1998The invention relates to the use of quinolone- and naphthyridonecarboxylic acid derivatives which a

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