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1035-80-9

(2-benzoylphenyl)(thiophen-2-yl)methanone is a ketone derivative with a molecular formula C18H13OS. It is composed of a benzene ring with a benzoyl group attached to one of the phenyl rings, and a thiophene ring attached to the other phenyl ring. This unique structure and properties make it a promising candidate for various applications in organic synthesis and medicinal chemistry.

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  • 1035-80-9 Structure

  • Basic information

    1. Product Name: (2-Benzoylphenyl)(thiophen-2-yl)Methanone
    2. Synonyms: (2-Benzoylphenyl)(thiophen-2-yl)Methanone
    3. CAS NO:1035-80-9
    4. Molecular Formula: C18H12O2S
    5. Molecular Weight: 292.35168
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1035-80-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (2-Benzoylphenyl)(thiophen-2-yl)Methanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2-Benzoylphenyl)(thiophen-2-yl)Methanone(1035-80-9)
    11. EPA Substance Registry System: (2-Benzoylphenyl)(thiophen-2-yl)Methanone(1035-80-9)

  • 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: 1035-80-9(Hazardous Substances Data)

1035-80-9 Usage

Uses

Used in Organic Synthesis:
(2-benzoylphenyl)(thiophen-2-yl)methanone is used as a key building block in organic synthesis for the preparation of various organic compounds. Its unique structure allows for the creation of a wide range of molecules with different properties and applications.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (2-benzoylphenyl)(thiophen-2-yl)methanone is used as a key building block for the preparation of various pharmaceuticals. Its unique structure and properties make it a valuable component in the development of new drugs with potential therapeutic effects.
Used in Drug Development:
(2-benzoylphenyl)(thiophen-2-yl)methanone has potential applications in the development of new drugs due to its unique structure and properties. It can be used as a starting material or intermediate in the synthesis of pharmaceutical compounds with novel mechanisms of action and therapeutic potential.
Used in Materials Science:
Additionally, (2-benzoylphenyl)(thiophen-2-yl)methanone may have applications in materials science, where its unique structure and properties can be utilized to develop new materials with specific characteristics for various industries.
Used in Research:
(2-benzoylphenyl)(thiophen-2-yl)methanone also has research applications in the study of organic reactions and mechanisms. Its unique structure allows researchers to investigate various chemical reactions and pathways, contributing to the understanding of organic chemistry and the development of new synthetic methods.

Check Digit Verification of cas no

The CAS Registry Mumber 1035-80-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,3 and 5 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1035-80:
(6*1)+(5*0)+(4*3)+(3*5)+(2*8)+(1*0)=49
49 % 10 = 9
So 1035-80-9 is a valid CAS Registry Number.

1035-80-9Relevant articles and documents

Regioselective annulation of unsymmetrical 1,2-phenylenebis(diaryl/diheteroarylmethanol): A facile synthesis of anthracene, tetracene, and naphtho[b]thiophene analogues

Sivasakthikumaran, Ramakrishnan,Rafiq, Settu Muhammad,Sankar, Elumalai,Clement, J. Arul,Mohanakrishnan, Arasambattu K.

, p. 7816 - 7835 (2015/12/31)

A systematic study on the regioselective cyclization of benzene- and naphthalene-based unsymmetrical diols with HBr (33 %) in acetic acid at room temperature led to the formation of annulation products. By using this method, synthesis of a wide variety of anthracene, tetracene and naphtho[b]thiophene analogues was achieved in good to excellent yields. By employing HBr (33 %) in acetic acid as a catalyst for regioselective cyclization of unsymmetrical diols was very facile and devoid of commonly encountered dihydroisobenzofuran formation. Regioselective cyclization of benzene- and naphthalene-based unsymmetrical diols with HBr (33 %) in acetic acid at room temperature led to the formation of annulated arenes and heteroarenes in good to excellent yields.

Oxidative cleavage of 1,3-disubstituted benzo[ c ]furans with activated manganese dioxide: A facile preparation of 1,2-Di(het)aroylbenzenes

Sivasakthikumaran, Ramakrishnan,Nandakumar, Meganathan,Mohanakrishnan, Arasambattu K.

supporting information, p. 1896 - 1900 (2014/08/18)

Manganese dioxide mediated oxidative cleavage of 1,3-disubstituted benzo[c]furans in dichloromethane at room temperature gave good yields of 1,2-di(het)aroylbenzenes. Georg Thieme Verlag Stuttgart. New York.

Oxidative ring opening of 1,3-diarylbenzo[c]heterocycles using m-CPBA: Preparation of 1,2-diaroylbenzenes

Nandakumar, Meganathan,Sivasakthikumaran, Ramakrishnan,Mohanakrishnan, Arasambattu K.

experimental part, p. 3647 - 3657 (2012/07/27)

An unprecedented oxidative cleavage of benzo[c]heterocycles using m-CPBA is reported. The reaction of 1,3-diaryl benzo[c]heterocycles with m-CPBA (meta-chloroperoxybenzoic acid) at room temperature for 5 min led to the formation of 1,2-diaroylbenzenes in good to excellent yields.

Synthesis of annulated arenes and heteroarenes involving lewis acid-mediated regioselective annulation of unsymmetrical 1,2-(Diaryl/ diheteroarylmethine)dipivalates

Sivasakthikumaran, Ramakrishnan,Nandakumar, Meganathan,Mohanakrishnan, Arasambattu K.

, p. 9053 - 9071,19 (2012/12/12)

A ZnBr2-mediated regioselective annulation of unsymmetrical 1,2-diarylmethinedipivalates in DCM at room temperature led to the formation of annulated arenes and heteroarenes. The annulation of the dipivalate proceeds through the intermediacy of

Copper-catalyzed benzylic C-H oxygenation under an oxygen atmosphere via N-H imines as an intramolecular directing group

Zhang, Line,Ang, Gim Yean,Chiba, Shunsuke

, p. 1622 - 1625 (2011/05/05)

Copper-catalyzed benzylic C-H oxygenation under an oxygen atmosphere was developed starting from carbonitriles and Grignard reagents via N-H imine intermediates. The present process is characterized by the following two-step sequence in a one-pot manner: (1) addition of Grignard reagents to carbonitriles to form N-H imines and (2) benzylic C-H oxygenation (C=O bond formation) triggered by 1,5-hydrogen atom transfer with transient iminyl copper species.

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