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1620511-30-9

4-(4-methoxyphenyl)pyridine-2,6-dicarbaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1620511-30-9 Structure

  • Basic information

    1. Product Name: 4-(4-methoxyphenyl)pyridine-2,6-dicarbaldehyde
    2. Synonyms: 4-(4-methoxyphenyl)pyridine-2,6-dicarbaldehyde
    3. CAS NO:1620511-30-9
    4. Molecular Formula:
    5. Molecular Weight: 241.246
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1620511-30-9.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: 4-(4-methoxyphenyl)pyridine-2,6-dicarbaldehyde(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(4-methoxyphenyl)pyridine-2,6-dicarbaldehyde(1620511-30-9)
    11. EPA Substance Registry System: 4-(4-methoxyphenyl)pyridine-2,6-dicarbaldehyde(1620511-30-9)

  • 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: 1620511-30-9(Hazardous Substances Data)

1620511-30-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1620511-30-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,2,0,5,1 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1620511-30:
(9*1)+(8*6)+(7*2)+(6*0)+(5*5)+(4*1)+(3*1)+(2*3)+(1*0)=109
109 % 10 = 9
So 1620511-30-9 is a valid CAS Registry Number.

1620511-30-9Downstream Products

1620511-30-9Relevant articles and documents

An efficient synthetic approach to 4′,5,5″-triaryl-2,2′:6′,2″-terpyridines

Kopchuk, Dmitry S.,Chepchugov, Nikolay V.,Kim, Grigory A.,Zyryanov, Grigory V.,Kovalev, Igor S.,Rusinov, Vladimir L.,Chupakhin, Oleg N.

supporting information, p. 296 - 299 (2016/01/12)

An efficient synthetic approach is proposed to construct 4′,5,5″-triaryl-2,2′:6′,2″-terpyridines using two methods of pyridine ring construction, that is, the Weiss method and the '1,2,4-triazine' methodology. Due to the use of '1,2,4-triazine' methodolog

Formation of a hetero[3]rotaxane by a dynamic component-swapping strategy

Wilson, Eleanor A.,Vermeulen, Nicolaas A.,McGonigal, Paul R.,Avestro, Alyssa-Jennifer,Sarjeant, Amy A.,Stern, Charlotte L.,Stoddart, J. Fraser

, p. 9665 - 9668 (2014/08/18)

Acid-catalysed scrambling of the mechanically interlocked components between two different homo[3]rotaxanes, constituted of dumbbells containing two secondary dialkylammonium ion recognition sites encircled by two [24]crown-8 rings, each containing a couple of imine bonds, affords a statistical mixture of a hetero[3]rotaxane along with the two homo[3]rotaxanes, indicating that neither selectivity nor cooperativity is operating during the assembly process. This journal is the Partner Organisations 2014.

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