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(S)-5-((S)-secbutyl)-1-(4-methoxybenzyl)pyrrolidine-2,4-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1258512-95-6 Structure
  • Basic information

    1. Product Name: (S)-5-((S)-secbutyl)-1-(4-methoxybenzyl)pyrrolidine-2,4-dione
    2. Synonyms: (S)-5-((S)-secbutyl)-1-(4-methoxybenzyl)pyrrolidine-2,4-dione
    3. CAS NO:1258512-95-6
    4. Molecular Formula:
    5. Molecular Weight: 275.348
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1258512-95-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (S)-5-((S)-secbutyl)-1-(4-methoxybenzyl)pyrrolidine-2,4-dione(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-5-((S)-secbutyl)-1-(4-methoxybenzyl)pyrrolidine-2,4-dione(1258512-95-6)
    11. EPA Substance Registry System: (S)-5-((S)-secbutyl)-1-(4-methoxybenzyl)pyrrolidine-2,4-dione(1258512-95-6)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1258512-95-6(Hazardous Substances Data)

1258512-95-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1258512-95-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,8,5,1 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1258512-95:
(9*1)+(8*2)+(7*5)+(6*8)+(5*5)+(4*1)+(3*2)+(2*9)+(1*5)=166
166 % 10 = 6
So 1258512-95-6 is a valid CAS Registry Number.

1258512-95-6Relevant articles and documents

Expanding the scope of oligo-pyrrolinone-pyrrolidines as protein-protein interface mimics

Raghuraman, Arjun,Xin, Dongyue,Perez, Lisa M.,Burgess, Kevin

, p. 4823 - 4833 (2013/07/05)

Oligo-pyrrolinone-pyrrolidines (generic structure 1) have the potential to interfere with protein-protein interactions (PPIs), but to reduce this to practice it is necessary to be able to synthesize these structures with a variety of different side chains

Tetramic acids and derivatives by telluride-triggered dieckmann cyclizations

Dittmer, Donald C.,Avilov, Dmitry V.,Kandula, Venkata Subbarao,Purzycki, Matthew T.,Martens, Zachary J.,Hohn, Elliot B.,Bacler, Matthew W.

experimental part, p. 61 - 83 (2010/09/10)

Treatment of α-bromoacyl amides of esters of N-protected α-amino acids with lithium telluride yields an amide enolate which cyclizes to unstable tetramic acids (2, 4-pyrrolidinediones) which can be converted to stable derivatives (e.g. enol esters, silyl enol ethers, enol tosylates). Reaction conditions are modified to reduce unwanted side reactions: protonation of the enolate, selfcatalyzed intermolecular aldol rections of the tetramic acids, and potential racemization at the α-carbon atom of the amino acid.

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