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34676-89-6

diphenylphosphide ion is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 34676-89-6 Structure

  • Basic information

    1. Product Name: diphenylphosphide ion
    2. Synonyms: diphenylphosphide ion
    3. CAS NO:34676-89-6
    4. Molecular Formula:
    5. Molecular Weight: 185.185
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 34676-89-6.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: diphenylphosphide ion(CAS DataBase Reference)
    10. NIST Chemistry Reference: diphenylphosphide ion(34676-89-6)
    11. EPA Substance Registry System: diphenylphosphide ion(34676-89-6)

  • 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: 34676-89-6(Hazardous Substances Data)

34676-89-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34676-89-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,6,7 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 34676-89:
(7*3)+(6*4)+(5*6)+(4*7)+(3*6)+(2*8)+(1*9)=146
146 % 10 = 6
So 34676-89-6 is a valid CAS Registry Number.

34676-89-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name diphenylphosphide ion

1.2 Other means of identification

Product number -
Other names diphenylphosphane, deprotonated form

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:34676-89-6 SDS

34676-89-6Relevant articles and documents

REACTION OF GEM-DIBROMOCYCLOPROPANES WITH DIPHENYLPHOSPHIDE ION

Meijs, Gordon F.

, p. 105 - 106 (2007/10/02)

Diphenylphosphide ion undergoes a photostimulated reaction with 7,7-dibromobicycloheptane and 1,1-dibromo-2,2,3,3-tetramethylcyclopropane involving both ionic and radical steps to afford cyclopropyldiphenylphosphines resulting from substitution and reduction.

Reaction of 1-Bromoadamantane with Diphenylphosphide and Diphenylarsenide Ions by the SRN1 Mechanism. Facile Nucleophilic Substitution at the Bridgehead Position

Rossi, Roberto A.,Palacios, Sara M.,Santiago, Ana N.

, p. 4654 - 4657 (2007/10/02)

The photostimulated reaction of 1-bromoadamantane (1) with diphenylphosphide (2) and diphenylarsenide (6) ions in liquid ammonia afforded good yields of the substitution products, together with small amounts of adamantane (4) and 1,1'-biadamantyl (5) as byproducts.The reaction of 1 with 2 in the dark did not occur, but stimulation with solvated electrons gives a small amount of the substitution product and 5, with a large amount of 4.The photostimulated reaction of 1 with 2 is inhibited by p-dinitrobenzene and di-tert-butyl nitroxide.All these results suggest that these reactions occur by the SRN1 mechanism of substitution, where radical and radical anions are intermediates.

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