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1031927-05-5

6,8-di-tert-butyl-3-phenylcoumarin is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1031927-05-5 Structure

  • Basic information

    1. Product Name: 6,8-di-tert-butyl-3-phenylcoumarin
    2. Synonyms: 6,8-di-tert-butyl-3-phenylcoumarin
    3. CAS NO:1031927-05-5
    4. Molecular Formula:
    5. Molecular Weight: 334.458
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1031927-05-5.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: 6,8-di-tert-butyl-3-phenylcoumarin(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6,8-di-tert-butyl-3-phenylcoumarin(1031927-05-5)
    11. EPA Substance Registry System: 6,8-di-tert-butyl-3-phenylcoumarin(1031927-05-5)

  • 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: 1031927-05-5(Hazardous Substances Data)

1031927-05-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1031927-05-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,1,9,2 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1031927-05:
(9*1)+(8*0)+(7*3)+(6*1)+(5*9)+(4*2)+(3*7)+(2*0)+(1*5)=115
115 % 10 = 5
So 1031927-05-5 is a valid CAS Registry Number.

1031927-05-5Downstream Products

1031927-05-5Relevant articles and documents

Pd-catalysed carbonylative annulation of salicylaldehydes with benzyl chlorides using N-formylsaccharin as a CO surrogate

Yadav, Vinod K.,Srivastava, Vishnu P.,Yadav, Lal Dhar S.

supporting information, p. 16281 - 16286 (2018/10/04)

A convenient and highly efficient Pd-catalysed carbonylative annulation of salicylaldehydes with benzyl chlorides to afford the corresponding 3-arylcoumarins in good to excellent yields has been developed. Importantly, the protocol utilizes a commercially available, low cost, solid and easy to handle N-formylsaccharin as an alternative to the highly toxic CO gas.

A complete switch of the directional selectivity in the annulation of 2-hydroxybenzaldehydes with alkynes

Zeng, Huiying,Li, Chao-Jun

supporting information, p. 13862 - 13865 (2015/01/09)

Controlling reaction selectivity is an eternal pursuit for chemists working in chemical synthesis. As part of this endeavor, our group has been exploring the possibility of constructing different natural product skeletons from the same simple starting mat

Synthesis of 3-arylcoumarins through N-heterocyclic carbene catalyzed condensation and annulation of 2-chloro-2-arylacetaldehydes with salicylaldehydes

Jiang, Yuansong,Chen, Wanzhi,Lu, Weimin

, p. 3669 - 3676 (2013/05/08)

The condensation reaction of 2-chloro-2-arylacetaldehyde with salicylaldehyde catalyzed by N-heterocyclic carbene (NHC) leading to 3-arylcoumarin was studied. A number of 3-arylcoumarin derivatives were obtained in good to excellent yields via this umpolung reaction. This reaction is facile and experimentally simple and mild.

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