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1-(2-fluorobenzyl)-1H-indole-5-carbaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 944893-62-3 Structure
  • Basic information

    1. Product Name: 1-(2-fluorobenzyl)-1H-indole-5-carbaldehyde
    2. Synonyms: Reaxys ID: 27110959;1-(2-fluorobenzyl)-1H-indole-5-carbaldehyde;1-[(2-fluorophenyl)methyl]-1H-indole-5-carbaldehyde;1H-Indole-5-carboxaldehyde, 1-[(2-fluorophenyl)methyl]-
    3. CAS NO:944893-62-3
    4. Molecular Formula: C16H12FNO
    5. Molecular Weight: 253.27
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 944893-62-3.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: 1-(2-fluorobenzyl)-1H-indole-5-carbaldehyde(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(2-fluorobenzyl)-1H-indole-5-carbaldehyde(944893-62-3)
    11. EPA Substance Registry System: 1-(2-fluorobenzyl)-1H-indole-5-carbaldehyde(944893-62-3)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 944893-62-3(Hazardous Substances Data)

944893-62-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 944893-62-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,4,8,9 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 944893-62:
(8*9)+(7*4)+(6*4)+(5*8)+(4*9)+(3*3)+(2*6)+(1*2)=223
223 % 10 = 3
So 944893-62-3 is a valid CAS Registry Number.

944893-62-3Relevant articles and documents

Synthesis of podophyllotoxin derivatives as potential antitumor agents

Sun, Yanjun,Chen, Hong,Hua, Huiming,Liu, Yongfeng,Zhang, Shi

, p. 408 - 413 (2014/08/18)

A series of novel podophyllotoxin derivatives was synthesized by coupling 4β-amino-4′-demethyl-4-desoxypodophyllotoxin (3a) or 4β-amino-4-desoxypodophyllotoxin (3b) with N-substituted 5-formylindole (2a-h). Their structures were identied by spectroscopic techniques. These novel derivatives were evaluated for cytotoxicity in vitro against HepG2 and HeLa cell lines. Compared with etoposide, most of the compounds showed more potent cytotoxicities against two tumor cell lines. Judging from the IC50 values, compound 5n is a promising agent, which is about 15 and 5 times more toxic than etoposide against HepG2 and HeLa cell lines, respectively.

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