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1-(7,7-dimethyl-2-oxobicyclo[2.2.1]hept-1-yl)-N-phenylmethanesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81617-83-6

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81617-83-6 Usage

Chemical class

Sulfonamide derivative

Structure

Bicyclic ketone with a phenylmethanesulfonamide group attached

Applications

Pharmaceutical research and drug development

Potential uses

Treatment of various medical conditions (requires further study and evaluation)

Functional groups

Sulfonyl group, amine group, bicyclic ketone

Molecular weight

315.41 g/mol (calculated from molecular formula)

Appearance

Unknown (requires experimental data)

Solubility

Unknown (requires experimental data)

Stability

Unknown (requires experimental data)

Reactivity

Unknown (requires experimental data)

Toxicity

Unknown (requires experimental data)

Environmental impact

Unknown (requires experimental data)

Synthesis

Not provided in the material, but typically synthesized through chemical reactions involving precursor compounds

Purity

Not provided in the material, but typically assessed through analytical techniques like chromatography or spectroscopy

Check Digit Verification of cas no

The CAS Registry Mumber 81617-83-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,6,1 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 81617-83:
(7*8)+(6*1)+(5*6)+(4*1)+(3*7)+(2*8)+(1*3)=136
136 % 10 = 6
So 81617-83-6 is a valid CAS Registry Number.

81617-83-6SDS

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 (1S)-2-oxo-bornane-sulfonanilide-(10)

1.2 Other means of identification

Product number -
Other names (1S)-2-Oxo-bornan-10-sulfonsaeure-anilid

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:81617-83-6 SDS

81617-83-6Relevant academic research and scientific papers

Synthesis of: N -arylsulfonamides via Fe-promoted reaction of sulfonyl halides with nitroarenes in an aqueous medium

Jiang, Jun,Zeng, Sheng,Chen, De,Cheng, Chaozhihui,Deng, Wei,Xiang, Jiannan

supporting information, p. 5016 - 5020 (2018/07/25)

A fascinating Fe-promoted protocol for the synthesis of N-arylsulfonamides has been developed. Starting from commercially available nitroarenes and sulfonyl chlorides, moderate to excellent yields of the corresponding N-arylsulfonamides can be obtained. In particular, Fe dust serves as the sole reductant in the transformation and it can be easily performed on a large scale.

Application in asymmetric Morita-Baylis-Hillman reactions

McIteka, Lulama P.,Lobb, Kevin A.,Kaye, Perry T.

, p. 151 - 163 (2016/10/22)

N-Substituted 2-exo-hydroxybornyl-10-sulfonamides, prepared as potential chiral auxiliaries for use in asymmetric Morita-Baylis-Hillman (MBH) reactions, have been treated with acryloyl chloride to afford the corresponding 2-exo-Acrylate esters as MBH subs

Camphorsulfonamide derivatives: A new class of chiral catalysts for the titanium alkoxide-promoted addition of dialkylzinc to aldehydes

Ramoen, Diego J.,Yus, Miguel

, p. 2479 - 2496 (2007/10/03)

The enantioselective addition of dialkylzinc to several aldehydes, using different chiral bidentate ligands (3a-j, 4a-h) [derived from (+)-10-camphorsulfonyl chloride] and titanium alkoxide as catalysts, is studied. The influence of temperature, titanium alkoxide, stoichiometry, additive, aldehyde and ligand structure is also studied.

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