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1273599-65-7

6-BroMo-7-Methoxy-indan-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1273599-65-7 Structure

  • Basic information

    1. Product Name: 6-BroMo-7-Methoxy-indan-1-one
    2. Synonyms: 6-BroMo-7-Methoxy-indan-1-one
    3. CAS NO:1273599-65-7
    4. Molecular Formula: C10H9BrO2
    5. Molecular Weight: 241.08126
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1273599-65-7.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: 6-BroMo-7-Methoxy-indan-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-BroMo-7-Methoxy-indan-1-one(1273599-65-7)
    11. EPA Substance Registry System: 6-BroMo-7-Methoxy-indan-1-one(1273599-65-7)

  • 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: 1273599-65-7(Hazardous Substances Data)

1273599-65-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1273599-65-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,7,3,5,9 and 9 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1273599-65:
(9*1)+(8*2)+(7*7)+(6*3)+(5*5)+(4*9)+(3*9)+(2*6)+(1*5)=197
197 % 10 = 7
So 1273599-65-7 is a valid CAS Registry Number.

1273599-65-7Downstream Products

1273599-65-7Relevant articles and documents

Divergent Synthetic Route to Oxidized Benzofulvene Sesquiterpenoids: Protecting-Group-Free Total Synthesis of Nicotianasesterpenes A, B, and a Polygonum Sesquiterpenoid

Jeong, Myeonggyo,Lee, Hyunkee,Kim, Gibeom,Jo, Jeyun,Chang, Jae Won,Jung, Jee H.,Suh, Young-Ger,Yun, Hwayoung

, p. 6714 - 6719 (2019)

A divergent approach toward the protecting-group-free total synthesis of oxidized benzofulvene sesquiterpenoids is described. Highlight of our synthesis includes regio- and stereoselective assembly of the common intermediate 9 by the orchestrated application of a Pd(0)-catalyzed reductive dehalogenation, a solvent-free methylenation, and a vinylogous Stork enamine aldol condensation in a substrate-controlled manner. The advanced intermediate 9 was efficiently transformed to nicotianasesterpenes A, B, and a polygonum sesquiterpenoid, respectively.

Rh-Catalyzed Annulation of Benzoic Acids, Formaldehyde, and Malonates via ortho-Hydroarylation to Indanones

Yu, Shuling,Lv, Ningning,Hong, Chao,Liu, Zhanxiang,Zhang, Yuhong

supporting information, p. 8354 - 8358 (2020/11/18)

A three-component reaction from readily available low-cost materials of benzoic acids, formaldehyde, and malonates for the preparation of indanones by rhodium catalysis is reported. The annulation is initiated by an ortho-hydroarylation of benzoic acids, and a Lewis acid is not required. The solvent has a significant influence to the reaction, and 2-substituted or nonsubstituted indanones are obtained by the change of solvent.

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