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187682-10-6

(+/-)-4-(3,4,5,6-tetrahydro-2H-pyran-2-yloxymethyl)benzaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 187682-10-6 Structure

  • Basic information

    1. Product Name: (+/-)-4-(3,4,5,6-tetrahydro-2H-pyran-2-yloxymethyl)benzaldehyde
    2. Synonyms: (+/-)-4-(3,4,5,6-tetrahydro-2H-pyran-2-yloxymethyl)benzaldehyde
    3. CAS NO:187682-10-6
    4. Molecular Formula:
    5. Molecular Weight: 220.268
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 187682-10-6.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-(3,4,5,6-tetrahydro-2H-pyran-2-yloxymethyl)benzaldehyde(CAS DataBase Reference)
    10. NIST Chemistry Reference: (+/-)-4-(3,4,5,6-tetrahydro-2H-pyran-2-yloxymethyl)benzaldehyde(187682-10-6)
    11. EPA Substance Registry System: (+/-)-4-(3,4,5,6-tetrahydro-2H-pyran-2-yloxymethyl)benzaldehyde(187682-10-6)

  • 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: 187682-10-6(Hazardous Substances Data)

187682-10-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 187682-10-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,7,6,8 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 187682-10:
(8*1)+(7*8)+(6*7)+(5*6)+(4*8)+(3*2)+(2*1)+(1*0)=176
176 % 10 = 6
So 187682-10-6 is a valid CAS Registry Number.

187682-10-6Relevant articles and documents

Carbene-Catalyzed Reductive Coupling of Nitrobenzyl Bromide and Nitroalkene via the Single-Electron-Transfer (SET) Process and Formal 1,4-Addition

Wang, Yuhuang,Du, Yu,Huang, Xuan,Wu, Xingxing,Zhang, Yuexia,Yang, Song,Chi, Yonggui Robin

supporting information, p. 632 - 635 (2017/02/10)

A carbene-catalyzed reductive 1,4-addition of nitrobenzyl bromides to nitroalkenes is disclosed. The reaction proceeds via a carbene-enabled single-electron-transfer process that generates radicals as key intermediates. The present study expands the potentials of carbene catalysis and offers unusual transformations for common substrates in organic synthesis.

Dendrimers consisting of stilbene or distyrylbenzene building blocks synthesis and stability

Lehmann, Matthias,Schartel, Bernhard,Hennecke, Manfred,Meier, Herbert

, p. 13377 - 13394 (2007/10/03)

On the basis of Wittig-Homer reactions and protection group techniques compound 7 for the core and the components 9a-c and 11a-c for the dendrons were prepared and linked in the final step. The convergent synthesis yielded constitutionally and configurationally pure dendrimers (2a-c, 2a'-c') which consist of distyrylbenzene units. Their thermo-oxidative stability in the presence of air was studied by chemiluminescence and compared to the dendrimers 1 consisting of stilbene units.

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