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1414969-71-3

C18H18N4O2S*ClH is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1414969-71-3 Structure

  • Basic information

    1. Product Name: C18H18N4O2S*ClH
    2. Synonyms: C18H18N4O2S*ClH
    3. CAS NO:1414969-71-3
    4. Molecular Formula:
    5. Molecular Weight: 390.893
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1414969-71-3.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: C18H18N4O2S*ClH(CAS DataBase Reference)
    10. NIST Chemistry Reference: C18H18N4O2S*ClH(1414969-71-3)
    11. EPA Substance Registry System: C18H18N4O2S*ClH(1414969-71-3)

  • 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: 1414969-71-3(Hazardous Substances Data)

1414969-71-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1414969-71-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,4,9,6 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1414969-71:
(9*1)+(8*4)+(7*1)+(6*4)+(5*9)+(4*6)+(3*9)+(2*7)+(1*1)=183
183 % 10 = 3
So 1414969-71-3 is a valid CAS Registry Number.

1414969-71-3Downstream Products

1414969-71-3Relevant articles and documents

Synthesis of retinoid enhancers based on 2-aminobenzothiazoles for anti-cancer therapy

Gardner, Christopher R.,Cheung, Belamy B.,Koach, Jessica,Black, David Stc.,Marshall, Glenn M.,Kumar, Naresh

, p. 6877 - 6884 (2012)

Indole-3-amides and dipeptides were produced from 2-aminobenzothiazoles using the PyBop peptide coupling reagent. These analogues were tested in anti-cancer cell viability assays against SH-SY5Y neuroblastoma and MDA-MB-231 breast adenocarcinoma cell lines, and were found to exhibit cytotoxic activities at concentrations ranging from 0.1 to 20 μM. These compounds were also found to act additively with a low dosage of 13-cis-retinoic acid in neuroblastoma cells. Then, using neuroblastoma cells transfected to stably overexpress the RARβ2 gene, a SAR was developed for the indole-3-amides. Real-time PCR was also used to demonstrate their RARβ2 agonistic activity.

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