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2-Propenenitrile, 3-(4-chlorophenyl)-2-[[(4-methylphenyl)sulfonyl]methyl]-, (2E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

594835-24-2

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594835-24-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 594835-24-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,9,4,8,3 and 5 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 594835-24:
(8*5)+(7*9)+(6*4)+(5*8)+(4*3)+(3*5)+(2*2)+(1*4)=202
202 % 10 = 2
So 594835-24-2 is a valid CAS Registry Number.

594835-24-2Downstream Products

594835-24-2Relevant academic research and scientific papers

Direct sulfonylation of Baylis-Hillman alcohols and diarylmethanols with TosMIC in ionic liquid-[Hmim]HSO4: An unexpected reaction

Garima,Srivastava, Vishnu P.,Yadav, Lal Dhar S.

experimental part, p. 4622 - 4626 (2011/09/21)

A Bronsted acidic ionic liquid-[Hmim]HSO4 promoted unexpected reaction of Baylis-Hillman alcohols and diarylmethanols with p-toluenesulfonylmethyl isocyanide (TosMIC) affording the corresponding sulfone derivatives instead of N-tosylmethyl amid

Synthesis of allyl aryl sulfone derivatives from Baylis-Hillman acetates in water

Karnakar, Konkala,Shankar, Jilla,Murthy, Sabbavarapu Narayana,Nageswar, Yadavalli Venkata Durga

experimental part, p. 875 - 880 (2011/06/27)

Various phenyl and p-tolyl allyl sulfone derivatives were prepared stereoselectively by reacting Baylis-Hillman acetates with sodium 4-R-benzenesulfinate (R=H, Me) in H2O. The reaction was very efficient in providing the corresponding sulfone d

An unexpected reaction of arenesulfonyl cyanides with allylic alcohols: Preparation of trisubstituted allyl sulfones

Reddy, Leleti Rajender,Hu, Bin,Prashad, Mahavir,Prasad, Kapa

experimental part, p. 172 - 174 (2009/04/10)

(Chemical Equation Presented) An efficient and practical protocol for the highly selective preparation of substituted allyl sulfones has been developed. Arenesulfonyl cyanides, Baylis-Hillman adducts, and simple allylic alcohols give an unforeseen outcome

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