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N-methyl-N-benzyl-2-(S)-amino-3-(3-indolyl)propionamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 169673-44-3 Structure
  • Basic information

    1. Product Name: N-methyl-N-benzyl-2-(S)-amino-3-(3-indolyl)propionamide
    2. Synonyms: N-methyl-N-benzyl-2-(S)-amino-3-(3-indolyl)propionamide
    3. CAS NO:169673-44-3
    4. Molecular Formula:
    5. Molecular Weight: 307.395
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 169673-44-3.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: N-methyl-N-benzyl-2-(S)-amino-3-(3-indolyl)propionamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-methyl-N-benzyl-2-(S)-amino-3-(3-indolyl)propionamide(169673-44-3)
    11. EPA Substance Registry System: N-methyl-N-benzyl-2-(S)-amino-3-(3-indolyl)propionamide(169673-44-3)
  • 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: 169673-44-3(Hazardous Substances Data)

169673-44-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 169673-44-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,6,7 and 3 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 169673-44:
(8*1)+(7*6)+(6*9)+(5*6)+(4*7)+(3*3)+(2*4)+(1*4)=183
183 % 10 = 3
So 169673-44-3 is a valid CAS Registry Number.

169673-44-3Relevant articles and documents

L-tryptophan urea amides as NK1/NK2 Dual antagonists

Qi, Hongbo,Shah, Shrenik K.,Cascieri, Margaret A.,Sadowski, Sharon J.,MaCcoss, Malcolm

, p. 2259 - 2262 (1998)

We report that a systematic modification of an NK1 receptor selective antagonist resulted in the identification of novel compounds, 4c and 4d, with high affinity for both NK1 and NK2 receptors.

TRYPTHOPHAN UREAS AS NEUROKINNIN ANTAGONISTS

-

, (2008/06/13)

Disclosed are Substituted azacycles of formula I STR1 are tachykinin receptor antagonists useful in the treatment of inflammatory diseases, pain or migraine, and asthma. In particular compounds of formula I are shown to be neurokinin antagonists.

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