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2H-Pyran-2-one, tetrahydro-6-phenyl-5-(phenylsulfonyl)-, cis- is a complex organic chemical compound with the molecular formula C16H16O3S. It is a derivative of 2H-pyran-2-one, featuring a tetrahydro structure, a phenyl group at the 6th position, and a phenylsulfonyl group at the 5th position. The cis- configuration indicates that the phenyl and phenylsulfonyl groups are on the same side of the molecule. 2H-Pyran-2-one, tetrahydro-6-phenyl-5-(phenylsulfonyl)-, cis- is characterized by its unique structure and properties, which may have potential applications in various chemical and pharmaceutical industries.

113519-11-2

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113519-11-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 113519-11-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,5,1 and 9 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 113519-11:
(8*1)+(7*1)+(6*3)+(5*5)+(4*1)+(3*9)+(2*1)+(1*1)=92
92 % 10 = 2
So 113519-11-2 is a valid CAS Registry Number.

113519-11-2SDS

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 cis-6-phenyl-5-(phenylsulfonyl)-3,4,5,6-tetrahydropyran-2-one

1.2 Other means of identification

Product number -
Other names -

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 -
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More Details:113519-11-2 SDS

113519-11-2Relevant academic research and scientific papers

Synthesis of γ-sulfonyl δ-lactones and β-sulfonyl styrenes

Chan, Chieh-Kai,Chen, Yu-Hsin,Hsu, Ru-Ting,Chang, Meng-Yang

, p. 46 - 54 (2016/12/09)

A facile route to the synthesis of γ-sulfonyl lactones 5 and β-sulfonyl styrenes 6 has been developed, achieving moderate to good yields via the (1) NaH mediated Michael addition of β-ketosulfones 3 and methyl acrylate in refluxing THF and (2) NaBH4mediated stereoselective reduction/lactonization of δ-ketoesters 4 in boiling MeOH, or (3) boron trifluoride etherate mediated ring-opening of lactones 5 in MeOH at reflux.

4-(Phenylsulfonyl)butanoic Acid. Preparation, Dianion Generation, and Application to Four-Carbon Chain Extension

Thompson, Charles M.,Frick, Jeffrey A.

, p. 890 - 896 (2007/10/02)

The bishomoenolate dianion of 4-(phenylsulfonyl)butanoic acid was investigated.It was observed the dianion could be generated in greater than 95percent yield with 200 mol percent of n-BuLi at certain concentrations.The dianion was reacted with a variety o

"REMOTE" DIANIONS-I. UTILITY OF 4-PHENYLSULFONYLBUTANOIC ACID IN THE MILD CONVERSION OF ALDEHYDES AND KETONES TO LACTONES.

Thompson, Charles M.

, p. 4243 - 4246 (2007/10/02)

Ketones and aldehydes are converted to lactones in high yield by stepwise treatment with the dianion of 4-phenylsulfonylbutanoic acid and trifluoroacetic anhydride.

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