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Bicyclo[2.2.1]hept-2-ene, 5-chloro-6-(phenylseleno)-, (5-endo,6-exo)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 74868-47-6 Structure
  • Basic information

    1. Product Name: Bicyclo[2.2.1]hept-2-ene, 5-chloro-6-(phenylseleno)-, (5-endo,6-exo)-
    2. Synonyms:
    3. CAS NO:74868-47-6
    4. Molecular Formula: C13H13ClSe
    5. Molecular Weight: 283.659
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 74868-47-6.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: Bicyclo[2.2.1]hept-2-ene, 5-chloro-6-(phenylseleno)-, (5-endo,6-exo)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Bicyclo[2.2.1]hept-2-ene, 5-chloro-6-(phenylseleno)-, (5-endo,6-exo)-(74868-47-6)
    11. EPA Substance Registry System: Bicyclo[2.2.1]hept-2-ene, 5-chloro-6-(phenylseleno)-, (5-endo,6-exo)-(74868-47-6)
  • 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: 74868-47-6(Hazardous Substances Data)

74868-47-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74868-47-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,8,6 and 8 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 74868-47:
(7*7)+(6*4)+(5*8)+(4*6)+(3*8)+(2*4)+(1*7)=176
176 % 10 = 6
So 74868-47-6 is a valid CAS Registry Number.

74868-47-6Downstream Products

74868-47-6Relevant articles and documents

Arylselenenation of conjugated dienes by arylselenenamides in the presence of phosphorus(V) oxyhalides

Antipin, Roman L.,Beloglazkina, Elena K.,Zyk, Nikolay V.,Zefirov, Nikolay S.

, p. 729 - 731 (2007)

Arylselenenation of conjugated and non-conjugated dienes by arylselenenamides in the presence of phosphorus(V) oxyhalides has been studied. Reactions with conjugated dienes lead to 1,4-adducts whilst only addition to double bonds takes place in reactions

Reactions of areneselenenamides with alkenes in the presence of phosphorus(V) and sulfur(IV) oxyhalides. New synthesis of β-Haloalkyl Selenides

Antipin,Klak,Beloglazkina,Zyk

experimental part, p. 842 - 847 (2009/12/09)

A new procedure was proposed for activation of areneselenenamides with phosphorus(V) and sulfur (IV) oxyhalides. According to the 1H, 13C, and 31P NMR data, areneselenenamide reacts with phosphorus oxyhalide to form interm

Electrophilic cleavage of cyclopropanes. The areneselenenylation of tetracyclo2,7.04,6>heptane (quadricyclene)

Beaulieu, Pierre L.,Morisset, Veronique M.,Garratt, Dennis G.

, p. 1005 - 1013 (2007/10/02)

The reaction of benzeneselenyl chloride with tetracyclo 3.2.0.02,7.04,6 heptane (quadricyclene) yields, under conditions of kinetic control, adducts of both 1,3-and conjugative 1,6-addition, the latter being formed preferentially.Ele

Factors influencing the nature of seleniranium ions in selenenyl chloride additions to alkenes: the use of methanol as solvent

Garratt, Dennis G.,Kabo, Ann

, p. 1030 - 1041 (2007/10/02)

The reaction of benzeneselenenyl chloride with some simple alkylsubstituted acyclic and cyclic alkenes has been investigated using methanol as the solvent.Products of solvent-incorporation , β-methoxyalkyl phenyl selenides, are normally favoured over the

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