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152420-81-0

5-chlorothieno[3,2-b]pyridine-3-carbaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 152420-81-0 Structure

  • Basic information

    1. Product Name: 5-chlorothieno[3,2-b]pyridine-3-carbaldehyde
    2. Synonyms: 5-chlorothieno[3,2-b]pyridine-3-carbaldehyde
    3. CAS NO:152420-81-0
    4. Molecular Formula: C8H4ClNOS
    5. Molecular Weight: 197.64146
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 152420-81-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 348.9±37.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.521±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: -2.36±0.40(Predicted)
    10. CAS DataBase Reference: 5-chlorothieno[3,2-b]pyridine-3-carbaldehyde(CAS DataBase Reference)
    11. NIST Chemistry Reference: 5-chlorothieno[3,2-b]pyridine-3-carbaldehyde(152420-81-0)
    12. EPA Substance Registry System: 5-chlorothieno[3,2-b]pyridine-3-carbaldehyde(152420-81-0)

  • 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: 152420-81-0(Hazardous Substances Data)

152420-81-0 Usage

Synthesis Reference(s)

Tetrahedron Letters, 34, p. 4249, 1993 DOI: 10.1016/S0040-4039(00)60540-3

Check Digit Verification of cas no

The CAS Registry Mumber 152420-81-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,2,4,2 and 0 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 152420-81:
(8*1)+(7*5)+(6*2)+(5*4)+(4*2)+(3*0)+(2*8)+(1*1)=100
100 % 10 = 0
So 152420-81-0 is a valid CAS Registry Number.

152420-81-0Downstream Products

152420-81-0Relevant articles and documents

Synthetic studies on N-acetyl derivatives of amino acids and thiolactone using Vilsmeier-haack reagent

Balasundaram,Venugopal,Perumal, Paramasivan T.

, p. 4249 - 4252 (1993)

A variety of N-acetyl derivatives of amino acids have been subjected to Vilsmeier reagent to obtain 2,4-dichloro-3,5-diformylpyrrole and 2-formylmethylene-4-substituted oxazolidin-5-ones. The N-acetyl homo cysteine thiolactone gave 5-chloro-3-formylthieno (2,3-b)pyridine on reaction with Vilsmeier reagent.

PYRAZOLO[1,5a]PYRIMIDINE DERIVATIVES AS IRAK4 MODULATORS

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Page/Page column 65, (2012/02/01)

Compounds of the formula I or II: wherein X, m, Ar, R1 and R2 are as defined herein. The subject compounds are useful for treatment of IRAK-mediated conditions.

ALPHA HELIX MIMETICS AND METHODS RELATING THERETO

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Page/Page column 102, (2009/12/28)

Alpha-helix mimetic structures and compounds represented by the formula (I) wherein the general formula and the definition of each symbol are as defined in the specification, a compound relating thereto, and methods relating thereto, are disclosed. Applic

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