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107551-92-8

3-amino-N-pyridin-4-ylpropanamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 107551-92-8 Structure

  • Basic information

    1. Product Name: 3-amino-N-pyridin-4-ylpropanamide
    2. Synonyms: 3-amino-N-pyridin-4-ylpropanamide;N-pyridin-4-yl-beta-alaninamide
    3. CAS NO:107551-92-8
    4. Molecular Formula: C8H11N3O
    5. Molecular Weight: 165.19244
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 107551-92-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3-amino-N-pyridin-4-ylpropanamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-amino-N-pyridin-4-ylpropanamide(107551-92-8)
    11. EPA Substance Registry System: 3-amino-N-pyridin-4-ylpropanamide(107551-92-8)

  • 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: 107551-92-8(Hazardous Substances Data)

107551-92-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107551-92-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,5,5 and 1 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 107551-92:
(8*1)+(7*0)+(6*7)+(5*5)+(4*5)+(3*1)+(2*9)+(1*2)=118
118 % 10 = 8
So 107551-92-8 is a valid CAS Registry Number.

107551-92-8Relevant articles and documents

One-pot optical resolution of oligopeptide helices through artificial peptide bundling

Guo, Yan-Ming,Oike, Hideaki,Saeki, Naoko,Aida, Takuzo

, p. 4915 - 4918 (2007/10/03)

The helical sense of the peptidic parts of a cyclodimeric zinc porphyrin host with helical oligopeptide units (1) determines whether a right- or left-handed oligopeptide guest (2) is selectively bound (see picture). In contrast, enantiomers of nonhelical

SYNTHESIS AND BIOLOGICAL ACTIVITY OF SOME NEW 4-(AMINOACYL)AMINOPYRIDINES AND 2-(AMINOACYL)AMINOPYRIMIDINE DERIVATIVES

El-Naggar, A. M.,Ahmed, F. S. M.,El-Salam, A. M. Abd,Latif, M. S. A.,El-Bary, H. M. Abd

, p. 1279 - 1285 (2007/10/02)

The synthesis of 4-(N-Tos and N-Pht-aminoacyl)aminopyridines and 2-(N-Tos and N-Pht-aminoacyl)aminopyrimidines has been achieved employing the acid chloride and carbodiimide methods.Hydrazinolysis of 4-(N-Pht-Gly or β-Ala)aminopyridines or 2-(N-Pht-L-Phe

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