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CAS

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1167445-32-0

4-((phenylselanyl)methyl)chromane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1167445-32-0 Structure

  • Basic information

    1. Product Name: 4-((phenylselanyl)methyl)chromane
    2. Synonyms: 4-((phenylselanyl)methyl)chromane
    3. CAS NO:1167445-32-0
    4. Molecular Formula:
    5. Molecular Weight: 303.262
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1167445-32-0.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: 4-((phenylselanyl)methyl)chromane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-((phenylselanyl)methyl)chromane(1167445-32-0)
    11. EPA Substance Registry System: 4-((phenylselanyl)methyl)chromane(1167445-32-0)

  • 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: 1167445-32-0(Hazardous Substances Data)

1167445-32-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1167445-32-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,7,4,4 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1167445-32:
(9*1)+(8*1)+(7*6)+(6*7)+(5*4)+(4*4)+(3*5)+(2*3)+(1*2)=160
160 % 10 = 0
So 1167445-32-0 is a valid CAS Registry Number.

1167445-32-0Downstream Products

1167445-32-0Relevant articles and documents

FeCl3-Catalyzed Regio-Divergent Carbosulfenylation of Unactivated Alkenes: Construction of a Medium-Sized Ring

Lv, Leiyang,Li, Zhiping

, p. 10985 - 10994 (2018)

A FeCl3-catalyzed regio-divergent carbosulfenylation of unactivated alkenes with electrophilic N-sulfenophthalimides has been developed. This protocol provides a straightforward and efficient access to various medium-sized rings, especially strained 7- and 8-membered carborings with a sulfur atom attached. The endo/exo selectivity in the reaction depends on the atom number of the chain between arene and alkene. Broad substrate scope, high yields, and gram-scale synthesis exemplified the utility and practicability of this protocol. In addition, this methodology can be extended to the carboselenylation of isolated alkenes.

Seleniranium ion-triggered reactions: New aspects of friedel-crafts and N-detosylative cyclizations

Lim, Hwan Jung,RajanBabu

supporting information; experimental part, p. 2924 - 2927 (2009/12/05)

Selenlranlum Ions at low temperatures (-90 to -78 0C) will initiate effective Frledel-Crafts cycllzatlon If a suitably placed arene is allowed to react even when the arene is unactivated. These intermediates generated from N-aryl-W-tosylamides undergo a n

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