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60211-80-5

3-Furancarboxaldehyde, 2,5-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 60211-80-5 Structure

  • Basic information

    1. Product Name: 3-Furancarboxaldehyde, 2,5-diphenyl-
    2. Synonyms:
    3. CAS NO:60211-80-5
    4. Molecular Formula: C17H12O2
    5. Molecular Weight: 248.281
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 60211-80-5.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: 3-Furancarboxaldehyde, 2,5-diphenyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-Furancarboxaldehyde, 2,5-diphenyl-(60211-80-5)
    11. EPA Substance Registry System: 3-Furancarboxaldehyde, 2,5-diphenyl-(60211-80-5)

  • 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: 60211-80-5(Hazardous Substances Data)

60211-80-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60211-80-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,2,1 and 1 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 60211-80:
(7*6)+(6*0)+(5*2)+(4*1)+(3*1)+(2*8)+(1*0)=75
75 % 10 = 5
So 60211-80-5 is a valid CAS Registry Number.

60211-80-5Relevant articles and documents

Rearrangement reaction synthesized 3-furan-carbaldehyde compound of silver catalytic epoxy compound and application of 3-furan-carbaldehyde compound

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Paragraph 0020; 0021; 0022; 0023, (2017/02/17)

The invention discloses a rearrangement reaction synthesized 3-furan-carbaldehyde compound of a silver catalytic epoxy compound and application of the 3-furan-carbaldehyde compound. The 3-furan-carbaldehyde compound can be obtained with a 1-formyl-2-acete

Synthesis of 3-Formylfurans via a Silver(I)-Catalyzed Epoxide Ring-Opening/1,2-Acyl Migration/Cyclization Cascade

Wang, Jing,Shen, Chen,Wang, Tao,Mo, Sheng,Li, Xingxin,Zhang, Zunting

, p. 3943 - 3948 (2016/12/30)

By the design of suitable starting materials, a silver(I)-catalyzed epoxide ring-opening/1,2-acyl migration/cyclization cascade has been developed, which allowed us to systematically prepare unsymmetrical 3-formylfurans. Various 3-formylfurans were prepared in good to excellent yields. In addition, the distinct fluorescence properties of 3-formylfurans in solution and the solid state are disclosed. (Figure presented.).

Synthesis of highly substituted 3-formylfurans by a gold(I)-catalyzed oxidation/1,2-alkynyl migration/cyclization cascade

Wang, Tao,Shi, Shuai,Hansmann, Max M.,Rettenmeier, Eva,Rudolph, Matthias,Hashmi, A. Stephen K.

, p. 3715 - 3719 (2014/04/17)

3-Formylfuran derivatives are core structures of a variety of bioactive natural products. However, procedures for their preparation are still rare and generally inefficient in terms of atom economy: These methods require multiple steps or harsh reaction c

Synthesis of fully substituted 3-formyl-4-iodofurans via a gold(I)-catalyzed oxidation/1,2-alkynyl migration/cyclization/iodination cascade

Wang, Tao,Shi, Shuai,Rudolph, Matthias,Hashmi, A. Stephen K.

supporting information, p. 2337 - 2342 (2014/07/21)

A highly efficient gold(I)-catalyzed cascade reaction for the synthesis of fully substituted 3-formyl-4-iodofurans has been developed. Mechanistic investigations indicate a reaction pathway that involves a direct iodination reaction of the organogold intermediate via functionalization of the Au=C(sp2) bond, instead of a direct iodination of the 3-formylfurans.

Pd/Cu-catalyzed cascade Sonogashira coupling/cyclization reactions to highly substituted 3-formyl furans

Yang, Jingyu,Wang, Chengyu,Xie, Xin,Li, Hongfeng,Li, Ende,Li, Yanzhong

supporting information; experimental part, p. 1342 - 1346 (2011/04/16)

An efficient palladium/copper-catalyzed approach to the synthesis of highly substituted 3-formyl furans from the reactions of readily available α-bromoenaminones with terminal alkynes has been developed. This methodology was realized by the cascade reactions of Sonogashira coupling and the subsequent intramolecular cyclization. The Royal Society of Chemistry 2011.

A brief synthesis of β-iodofurans

Bew, Sean P.,Knight, David W.

, p. 1007 - 1008 (2007/10/03)

5-Endo-dig iodocyclisations of alk-3-yn-1,2-diols 4, followed by in situ dehydration, lead to good yields of β-iodofurans 5, which can subsequently be converted into a wide range of derivatives 6-13, using transition metal-catalysed coupling reactions or

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