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  • 1627210-18-7 Structure
  • Basic information

    1. Product Name: C17H12BrNO2
    2. Synonyms: C17H12BrNO2
    3. CAS NO:1627210-18-7
    4. Molecular Formula:
    5. Molecular Weight: 342.192
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1627210-18-7.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: C17H12BrNO2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C17H12BrNO2(1627210-18-7)
    11. EPA Substance Registry System: C17H12BrNO2(1627210-18-7)
  • 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: 1627210-18-7(Hazardous Substances Data)

1627210-18-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1627210-18-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,2,7,2,1 and 0 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1627210-18:
(9*1)+(8*6)+(7*2)+(6*7)+(5*2)+(4*1)+(3*0)+(2*1)+(1*8)=137
137 % 10 = 7
So 1627210-18-7 is a valid CAS Registry Number.

1627210-18-7Downstream Products

1627210-18-7Relevant articles and documents

Isocyanide-based multicomponent reactions: Concise synthesis of spirocyclic oxindoles with molecular complexity by using a [1,5]-hydrogen shift as the key step

Su, Shikuan,Li, Chunju,Jia, Xueshun,Li, Jian

supporting information, p. 5905 - 5909 (2014/05/20)

A concise multicomponent reaction of isocyanide, α-substituted allenoate, and methyleneindolinone has been disclosed. This protocol provides a fast and straightforward approach to synthesize unusual tricyclic oxindoles in an efficient and atom-economic manner. Mechanistically, the present cycloaddition may proceed through a cascade sequence involving double Michael addition, double cyclization, double [1,5]-hydrogen shift, and group migration. The introduction of a special alkyl group to the allenoate is believed to play a key role in the cascade reaction. This method also features a broad substrate scope, which is particularly useful for the delivery of a large number of compounds. Shift your perspective! An unprecedented cascade reaction, under mild conditions, involving a double Michael addition, double cyclization, and double [1,5]-hydrogen shift, followed by group migration is disclosed. This reaction offers a fast and straightforward approach to unusual polycyclic spirooxindoles (see scheme).

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