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100316-78-7

DL-Phe-NHi-Pr is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 100316-78-7 Structure

  • Basic information

    1. Product Name: DL-Phe-NHi-Pr
    2. Synonyms:
    3. CAS NO:100316-78-7
    4. Molecular Formula:
    5. Molecular Weight: 206.288
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 100316-78-7.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: DL-Phe-NHi-Pr(CAS DataBase Reference)
    10. NIST Chemistry Reference: DL-Phe-NHi-Pr(100316-78-7)
    11. EPA Substance Registry System: DL-Phe-NHi-Pr(100316-78-7)

  • 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: 100316-78-7(Hazardous Substances Data)

100316-78-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100316-78-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,3,1 and 6 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 100316-78:
(8*1)+(7*0)+(6*0)+(5*3)+(4*1)+(3*6)+(2*7)+(1*8)=67
67 % 10 = 7
So 100316-78-7 is a valid CAS Registry Number.

100316-78-7Relevant articles and documents

ENANTIOMERIC QUANTIFICATIONS OF AMINO ACIDS THROUGH THEIR Nα-ACYL AMIDES BY GAS CHROMATOGRAPHY.

Hosten, N.,Anteunis, M. J. O.

, p. 45 - 47 (2007/10/02)

Apparent separation of 1.1 or higher on Chiralsil Val III can be obtained for Nα-acyl N-alkyl aminoacid amides allowing the use of short capillary gas chromatographic columns.A clean derivatization protocol without racemization is described, proceding through the NCA derivatives that are prepared from "in situ" silylated amino acids with trimethylsilyl cyanide.

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