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1401071-02-0

2-((2-hydroxy-5-nonylbenzyloxy)methoxy)-5-nonylbenzaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1401071-02-0 Structure

  • Basic information

    1. Product Name: 2-((2-hydroxy-5-nonylbenzyloxy)methoxy)-5-nonylbenzaldehyde
    2. Synonyms:
    3. CAS NO:1401071-02-0
    4. Molecular Formula:
    5. Molecular Weight: 510.758
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1401071-02-0.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: 2-((2-hydroxy-5-nonylbenzyloxy)methoxy)-5-nonylbenzaldehyde(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-((2-hydroxy-5-nonylbenzyloxy)methoxy)-5-nonylbenzaldehyde(1401071-02-0)
    11. EPA Substance Registry System: 2-((2-hydroxy-5-nonylbenzyloxy)methoxy)-5-nonylbenzaldehyde(1401071-02-0)

  • 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: 1401071-02-0(Hazardous Substances Data)

1401071-02-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1401071-02-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,1,0,7 and 1 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1401071-02:
(9*1)+(8*4)+(7*0)+(6*1)+(5*0)+(4*7)+(3*1)+(2*0)+(1*2)=80
80 % 10 = 0
So 1401071-02-0 is a valid CAS Registry Number.

1401071-02-0Downstream Products

1401071-02-0Relevant articles and documents

One-pot formylation and dimerization of p-alkyl phenols using DCMT-activated DMSO

Chu, Guobiao,Yu, Zhifang,Gao, Feng,Li, Chunbao

, p. 44 - 51 (2013)

Dimerization and formylation of p-alkyl-substituted phenols have been successfully achieved in one pot, using 2,4-dichloro-6-methoxy[1,3,5]triazine (DCMT)-activated dimethylsulfoxide. Similarly, the d5-labeled products have been prepared in high selectivity. To the best of our knowledge, the products are of new skeletons, which have not been reported to date. A plausible mechanism is proposed based on the experiments. Copyright Taylor & Francis Group, LLC.

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