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478659-08-4

(+)-methyl N'-(t-butyloxycarbonyl)-L-phenylalanyl-N-methylglycinate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 478659-08-4 Structure

  • Basic information

    1. Product Name: (+)-methyl N'-(t-butyloxycarbonyl)-L-phenylalanyl-N-methylglycinate
    2. Synonyms: (+)-methyl N'-(t-butyloxycarbonyl)-L-phenylalanyl-N-methylglycinate
    3. CAS NO:478659-08-4
    4. Molecular Formula:
    5. Molecular Weight: 350.415
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 478659-08-4.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'-(t-butyloxycarbonyl)-L-phenylalanyl-N-methylglycinate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (+)-methyl N'-(t-butyloxycarbonyl)-L-phenylalanyl-N-methylglycinate(478659-08-4)
    11. EPA Substance Registry System: (+)-methyl N'-(t-butyloxycarbonyl)-L-phenylalanyl-N-methylglycinate(478659-08-4)

  • 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: 478659-08-4(Hazardous Substances Data)

478659-08-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 478659-08-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,8,6,5 and 9 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 478659-08:
(8*4)+(7*7)+(6*8)+(5*6)+(4*5)+(3*9)+(2*0)+(1*8)=214
214 % 10 = 4
So 478659-08-4 is a valid CAS Registry Number.

478659-08-4Relevant articles and documents

Efficient microwave assisted syntheses of 2,5-diketopiperazines in aqueous media

Perez-Picaso, Lemuel,Escalante, Jaime,Olivo, Horacio F.,Rios, Maria Yolanda

experimental part, p. 2836 - 2849 (2009/12/06)

Aqueous in situ one-pot N-Boc-deprotection-cyclization of Nα-Boc-dipeptidyltert-butyl and methyl esters under microwave irradiation afforded 2,5-diketopiperazines (DKPs) in excellent yields. This protocol is rapid, safe, environmentally friendly, and high

Acid-promoted reactions in 1-hydroxy, 1-dimethylaminomethyl and 1-methylene-4-arylmethyl-2,4-dihydro-1H-pyrazino[2,1-b]quinazoline-3,6-diones

Heredia, María Luisa,De la Cuesta, Elena,Avenda?o, Carmen

, p. 6163 - 6170 (2007/10/03)

The 1-dimethylaminomethyl or 1-methylene group of the title compounds was introduced through a Mannich or a tandem of Mannich-Hofmann reactions as the final step of a protocol that is shorter than other previously described for these precursors of N-acyliminium species. In these compounds, the acid-promoted intramolecular cyclizations of Pictet-Spengler-type were restricted to the N(2)-unsubstituted compounds, while their N(2)-methyl substituted analogues gave instead dimerization products. The cyclization was effective with 1-hydroxy-1,2-disubstituted compounds, which were obtained through addition of a Grignard reagent to 2H,4H-pyrazino[2,1-b]quinazoline-1,3,6-triones.

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