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2,5-Pyrrolidinedione,3-ethyl-1-phenyl-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

588672-40-6

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588672-40-6 Usage

Chemical Class

Pyrrolidine-2,5-diones

Physical State

White solid

Solubility

Insoluble in water

Melting Point

119-121°C

Uses

Pharmaceutical Industry: Intermediate in drug synthesis
Organic Synthesis: Building block for chemical production

Toxicity

Low

Hazards

No significant hazards associated with its use

Check Digit Verification of cas no

The CAS Registry Mumber 588672-40-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,8,8,6,7 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 588672-40:
(8*5)+(7*8)+(6*8)+(5*6)+(4*7)+(3*2)+(2*4)+(1*0)=216
216 % 10 = 6
So 588672-40-6 is a valid CAS Registry Number.

588672-40-6Downstream Products

588672-40-6Relevant academic research and scientific papers

C(sp3)-H functionalizations of light hydrocarbons using decatungstate photocatalysis in flow

Deng, Yuchao,Fagnoni, Maurizio,Guthrie, Duncan,Laudadio, Gabriele,No?l, Timothy,Nun?, Manuel,Ravelli, Davide,Sun, Yuhan,Wal, Klaas Van Der

, p. 92 - 96 (2020/09/03)

Direct activation of gaseous hydrocarbons remains a major challenge for the chemistry community. Because of the intrinsic inertness of these compounds, harsh reaction conditions are typically required to enable C(sp3)-H bond cleavage, barring potential applications in synthetic organic chemistry. Here, we report a general and mild strategy to activate C(sp3)-H bonds in methane, ethane, propane, and isobutane through hydrogen atom transfer using inexpensive decatungstate as photocatalyst at room temperature. The corresponding carbon-centered radicals can be effectively trapped by a variety of Michael acceptors, leading to the corresponding hydroalkylated adducts in good isolated yields and high selectivity (38 examples).

Conjugate addition of nitroalkanes to N-substituted maleimides. Synthesis of 3-alkylsuccinimides and pyrrolidines

Ballini, Roberto,Bosica, Giovanna,Cioci, Gianluca,Fiorini, Dennis,Petrini, Marino

, p. 3603 - 3608 (2007/10/03)

3-Alkylidenesuccinimides obtained by conjugate addition of nitroalkanes to N-substituted maleimides can be reduced to the corresponding 3-alkyl derivatives by catalytic hydrogenation. 3-Alkylsuccinimides can be further reduced using BH3·Me

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