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Benzenesulfonamide, 2,4,6-trimethyl-N-[(1S)-1-(1-methylethyl)-2,3-butadienyl]-N-[(2E)-3-phen yl-2-propenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

597540-82-4

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597540-82-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 597540-82-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,9,7,5,4 and 0 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 597540-82:
(8*5)+(7*9)+(6*7)+(5*5)+(4*4)+(3*0)+(2*8)+(1*2)=204
204 % 10 = 4
So 597540-82-4 is a valid CAS Registry Number.

597540-82-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(1S)-1-isopropylbuta-2,3-dienyl]-2,4,6-trimethyl-N-[(E)-3-phenyl-2-propenyl]phenylsulfonamide

1.2 Other means of identification

Product number -
Other names N-((S)-1-Isopropyl-buta-2,3-dienyl)-2,4,6-trimethyl-N-((E)-3-phenyl-allyl)-benzenesulfonamide

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:597540-82-4 SDS

597540-82-4Relevant academic research and scientific papers

A highly regio- and stereoselective formation of bicyclo[4.2.0]oct-5-ene derivatives through thermal intramolecular [2 + 2] cycloaddition of allenes

Ohno, Hiroaki,Mizutani, Tsuyoshi,Kadoh, Yoichi,Aso, Akimasa,Miyamura, Kumiko,Fujii, Nobutaka,Tanaka, Tetsuaki

, p. 4378 - 4389 (2008/02/05)

(Chemical Equation Presented) Thermal [2 + 2] cycloaddition of allenes with an additional multiple bond is described. By simply heating the allenenes or allenynes having a three-atom tether in an appropriate solvent such as dioxane or DMF, the distal doub

Palladium(0)-catalyzed tandem cyclization of alleneues: Direct construction of tricyclic heterocycles through aromatic C-H activation

Ohno, Hiroaki,Miyamura, Kumiko,Mizutani, Tsuyoshi,Kadoh, Yoichi,Takeoka, Yusuke,Hamaguchi, Hisao,Tanaka, Tetsuaki

, p. 3728 - 3741 (2007/10/03)

Palladium(0)-catalyzed tandem cyclization of allenenes is described. Treatment of allenenes with an aryl halide, potassium carbonate, and catalytic [Pd(PPh3)4] in dioxane afforded tri- or tetracyclic heterocycles in moderate to good

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