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CAS

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1362860-55-6

2-((2S,4S)-2-cyclohexyl-1,3-dioxolan-4-yl)-1-(thiophen-2-yl)ethanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1362860-55-6 Structure

  • Basic information

    1. Product Name: 2-((2S,4S)-2-cyclohexyl-1,3-dioxolan-4-yl)-1-(thiophen-2-yl)ethanone
    2. Synonyms:
    3. CAS NO:1362860-55-6
    4. Molecular Formula:
    5. Molecular Weight: 280.388
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1362860-55-6.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: 2-((2S,4S)-2-cyclohexyl-1,3-dioxolan-4-yl)-1-(thiophen-2-yl)ethanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-((2S,4S)-2-cyclohexyl-1,3-dioxolan-4-yl)-1-(thiophen-2-yl)ethanone(1362860-55-6)
    11. EPA Substance Registry System: 2-((2S,4S)-2-cyclohexyl-1,3-dioxolan-4-yl)-1-(thiophen-2-yl)ethanone(1362860-55-6)

  • 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: 1362860-55-6(Hazardous Substances Data)

1362860-55-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1362860-55-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,2,8,6 and 0 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1362860-55:
(9*1)+(8*3)+(7*6)+(6*2)+(5*8)+(4*6)+(3*0)+(2*5)+(1*5)=166
166 % 10 = 6
So 1362860-55-6 is a valid CAS Registry Number.

1362860-55-6Downstream Products

1362860-55-6Relevant articles and documents

Asymmetric cycloetherifications by bifunctional aminothiourea catalysts: The importance of hydrogen bonding

Fukata, Yukihiro,Miyaji, Ryota,Okamura, Takaaki,Asano, Keisuke,Matsubara, Seijiro

, p. 1627 - 1634 (2013/07/27)

Chiral oxacyclic frameworks are prevalent in many natural products and bioactive compounds. In addition, a number of them are important synthetic intermediates. Thus, the synthesis of such structures is a significant goal in the field of organic chemistry. However, the development of catalytic asymmetric cycloetherification for the straightforward synthesis of these compounds remains a challenge. In this study, we propose the use of aminothiourea catalysis as an effective way to accomplish such a challenge. The asymmetric synthesis of chiral oxygen heterocycles, including tetrahydrofurans, tetrahydropyrans, and 1,3-dioxolanes, is demonstrated herein using intramolecular oxy-Michael addition mediated by bifunctional aminothiourea catalysts. Georg Thieme Verlag Stuttgart · New York.

Asymmetric synthesis of 1,3-dioxolanes by organocatalytic formal [3 + 2] cycloaddition via hemiacetal intermediates

Asano, Keisuke,Matsubara, Seijiro

supporting information; experimental part, p. 1620 - 1623 (2012/06/05)

A novel asymmetric formal [3 + 2] cycloaddition reaction for the synthesis of 1,3-dioxolanes using cinchona-alkaloid-thiourea-based bifunctional organocatalysts is reported. The reaction proceeds via the formation of hemiacetal intermediates between γ-hyd

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