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67502-51-6

Phosphonic acid, [(phenylseleno)methyl]-, diethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 67502-51-6 Structure

  • Basic information

    1. Product Name: Phosphonic acid, [(phenylseleno)methyl]-, diethyl ester
    2. Synonyms:
    3. CAS NO:67502-51-6
    4. Molecular Formula: C11H17O3PSe
    5. Molecular Weight: 307.188
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 67502-51-6.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: Phosphonic acid, [(phenylseleno)methyl]-, diethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Phosphonic acid, [(phenylseleno)methyl]-, diethyl ester(67502-51-6)
    11. EPA Substance Registry System: Phosphonic acid, [(phenylseleno)methyl]-, diethyl ester(67502-51-6)

  • 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: 67502-51-6(Hazardous Substances Data)

67502-51-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67502-51-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,5,0 and 2 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 67502-51:
(7*6)+(6*7)+(5*5)+(4*0)+(3*2)+(2*5)+(1*1)=126
126 % 10 = 6
So 67502-51-6 is a valid CAS Registry Number.

67502-51-6Relevant articles and documents

Direct and straightforward transfer of C1 functionalized synthons to phosphorous electrophiles for accessinggem-P-containing methanes

Touqeer, Saad,Ielo, Laura,Miele, Margherita,Urban, Ernst,Holzer, Wolfgang,Pace, Vittorio

supporting information, p. 2425 - 2429 (2021/04/02)

The direct transfer of different α-substituted methyllithium reagents to chlorinated phosphorous electrophiles of diverse oxidation state (phosphates, phosphine oxides and phosphines) is proposed as an effective strategy to synthesize geminal P-containing

DIETHYL-1-MAGNESIUM CHLORIDE METHANEPHOSPHONATE, A NOVEL GRIGNARD REAGENT AND ITS USE IN ORGANIC SYNTHESIS

Coutrot, P.,Youssefi-Tabrizi, M.,Grison, C.

, p. 13 - 18 (2007/10/02)

Diethyl-1-magnesium chloride methanephosphonate was obtained by an exchange reaction between diethyliodo methanephosphonate and isopropylmagnesium chloride in THF at -70 deg.C.Reactions of this novel Grignard reagent with various electrophiles are described, and compared with those of the analogous lithium or copper derivatives.Diethyl-1-magnesium chloride methanephosphonate is especially reactive towards phenylselenium halides and halogens.

ULTRASONIC FORMATION AND REACTIONS OF SODIUM PHENYLSELENIDE

Ley, Steven V.,O'Neil, Ian A.,Low, Caroline M. R.

, p. 5363 - 5368 (2007/10/02)

Treatment of diphenyldiselenide with sodium metal in tetrahydrofuran under ultrasonic conditions conveniently gave a suspension of sodium phenylselenide which could be transferred by syringe or cannula and reacted with sulphonates, halides and epoxides.

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