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N-allyl N-(4-chlorophenyl)acrylamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

340011-50-9

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340011-50-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 340011-50-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,0,0,1 and 1 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 340011-50:
(8*3)+(7*4)+(6*0)+(5*0)+(4*1)+(3*1)+(2*5)+(1*0)=69
69 % 10 = 9
So 340011-50-9 is a valid CAS Registry Number.

340011-50-9Downstream Products

340011-50-9Relevant academic research and scientific papers

Fused ring compound and preparation method thereof

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Paragraph 0079; 0085-0086, (2021/09/21)

The invention provides a fused ring compound and a preparation method thereof. In the method, precursor compounds A and B prepared under the conditions of triethylamine as a base, DMF as a solvent andpalladium acetate and triphenylphosphine as a catalyst react to generate a series of new fused ring compounds with a unique stereoselectivity. Compared with the conventional fused ring compound, thefused ring compound prepared by the invention has a more complicated structure, a mild reaction condition and a high reaction yield. The fused ring compound also shows a broader prospect of use in chemical production and clinical medicine.

A new route to N-aryl 2-alkenamides, N-allyl N-aryl 2-alkenamides, and N-aryl α,β-unsaturated γ-lactams from N-aryl 3-(phenylsulfonyl)propanamides

Wang, Eng-Chi,Huang, Keng-Shiang,Lin, Gwo-Woei,Lin, Jia-Ruei,Hsu, Ming-Kun

, p. 83 - 90 (2007/10/03)

A series of N-aryl 2-alkenamides were produced efficiently by treating N-aryl 3-(phenylsulfonyl)-propanamides with potassium tert-butoxide in THF at 0°C. Without isolation, it was further treated with an additional equivalent of potassium tert-butoxide and allyl bromide to give N-allyl N-aryl 2-alkenamides in one pot in good yields. Followed by a ring-closing metathesis reaction, these N-allyl N-aryl 2-alkenamides were respectively converted into corresponding N-aryl α,β-unsaturated γ-lactams in moderate yields.

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