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182123-50-8

2-CHLORO-N-(2-FORMYL-1H-INDOL-3-YL)-N-PHENYLACETAMIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 182123-50-8 Structure

  • Basic information

    1. Product Name: 2-CHLORO-N-(2-FORMYL-1H-INDOL-3-YL)-N-PHENYLACETAMIDE
    2. Synonyms: 2-CHLORO-N-(2-FORMYL-1H-INDOL-3-YL)-N-PHENYLACETAMIDE
    3. CAS NO:182123-50-8
    4. Molecular Formula: C17H13ClN2O2
    5. Molecular Weight: 312.75
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 182123-50-8.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: 2-CHLORO-N-(2-FORMYL-1H-INDOL-3-YL)-N-PHENYLACETAMIDE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-CHLORO-N-(2-FORMYL-1H-INDOL-3-YL)-N-PHENYLACETAMIDE(182123-50-8)
    11. EPA Substance Registry System: 2-CHLORO-N-(2-FORMYL-1H-INDOL-3-YL)-N-PHENYLACETAMIDE(182123-50-8)

  • 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: 182123-50-8(Hazardous Substances Data)

182123-50-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 182123-50-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,2,1,2 and 3 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 182123-50:
(8*1)+(7*8)+(6*2)+(5*1)+(4*2)+(3*3)+(2*5)+(1*0)=108
108 % 10 = 8
So 182123-50-8 is a valid CAS Registry Number.

182123-50-8Relevant articles and documents

Synthesis and study of some properties of 1-aryl-2-oxo-1,2,3,6- tetrahydro[1,4]diazepino[6,5-b]indole 4-oxides

Ryabova,Rastorgueva,Lisitsa,Alekseeva,Granik

, p. 1386 - 1398 (2007/10/03)

A number of 1-aryl-2-oxo-1,2,3,6-tetrahydro[1,4]diazepirio[6,5-b]indole 4-oxides were synthesized based on 3-[N-aryl-N-(chloroacetyl)amino]-2- formylindoles. The nature of the substituent in the 1-aryl fragment has a pronounced influence on the course of reactions throughout the whole sequence of transformations during the synthesis of diazepinoindoles. The reduction of 4-oxides by formamidinosulfinic acid, hydrogen in the presence of Pd/C, and sodium bisulfite was studied. The structures of the reaction products were confirmed using IR and 1H NMR spectroscopy and mass spectrometry.

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