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methyl N-(tert-butoxycarbonyl)-5,5-dimethyl-3-phenyl-Δ2-pyrroline-2-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1426680-68-3 Structure
  • Basic information

    1. Product Name: methyl N-(tert-butoxycarbonyl)-5,5-dimethyl-3-phenyl-Δ2-pyrroline-2-carboxylate
    2. Synonyms: methyl N-(tert-butoxycarbonyl)-5,5-dimethyl-3-phenyl-Δ2-pyrroline-2-carboxylate
    3. CAS NO:1426680-68-3
    4. Molecular Formula:
    5. Molecular Weight: 331.412
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1426680-68-3.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: methyl N-(tert-butoxycarbonyl)-5,5-dimethyl-3-phenyl-Δ2-pyrroline-2-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl N-(tert-butoxycarbonyl)-5,5-dimethyl-3-phenyl-Δ2-pyrroline-2-carboxylate(1426680-68-3)
    11. EPA Substance Registry System: methyl N-(tert-butoxycarbonyl)-5,5-dimethyl-3-phenyl-Δ2-pyrroline-2-carboxylate(1426680-68-3)
  • 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: 1426680-68-3(Hazardous Substances Data)

1426680-68-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1426680-68-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,6,6,8 and 0 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1426680-68:
(9*1)+(8*4)+(7*2)+(6*6)+(5*6)+(4*8)+(3*0)+(2*6)+(1*8)=173
173 % 10 = 3
So 1426680-68-3 is a valid CAS Registry Number.

1426680-68-3Downstream Products

1426680-68-3Relevant articles and documents

Synthesis of racemic δ,δ-dimethylproline derivatives

Rodriguez, Isabel,Calaza, M. Isabel,Cativiela, Carlos

, p. 1093 - 1099 (2013/03/28)

A versatile methodology for the preparation of racemic δ,δ- dimethylproline derivatives has been developed. Methyl N-Boc-δ,δ- dimethylprolinate was synthesized from a β-amino acid in six steps and 55 % overall yield. The route is amenable to the preparation of a broad range of δ,δ-disubstituted prolines by starting with the adequate β-amino acids. In addition, one of the intermediate compounds in the synthetic route has been used for the preparation of a δ,δ- dimethylproline derivative that is substituted at the β-position with a phenyl group. This has been achieved by coupling phenylboronic acid with a regioselectively generated vinyl triflate followed by a stereoselective hydrogenation. δ,δ-Dimethylproline derivatives have been efficiently synthesized by employing a β-amino acid as the starting material. The methodology is amenable to the preparation of other δ,δ- disubstituted prolines. Copyright

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