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2-Phenylphen-1-oxydichlorphosphan is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 33771-47-0 Structure
  • Basic information

    1. Product Name: 2-Phenylphen-1-oxydichlorphosphan
    2. Synonyms: 2-Phenylphen-1-oxydichlorphosphan
    3. CAS NO:33771-47-0
    4. Molecular Formula:
    5. Molecular Weight: 271.083
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 33771-47-0.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: 2-Phenylphen-1-oxydichlorphosphan(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Phenylphen-1-oxydichlorphosphan(33771-47-0)
    11. EPA Substance Registry System: 2-Phenylphen-1-oxydichlorphosphan(33771-47-0)
  • 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: 33771-47-0(Hazardous Substances Data)

33771-47-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33771-47-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,7,7 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 33771-47:
(7*3)+(6*3)+(5*7)+(4*7)+(3*1)+(2*4)+(1*7)=120
120 % 10 = 0
So 33771-47-0 is a valid CAS Registry Number.

33771-47-0SDS

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 2-Phenylphen-1-oxydichlorphosphan

1.2 Other means of identification

Product number -
Other names phosphorodichloridous acid biphenyl-2-yl ester

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:33771-47-0 SDS

33771-47-0Upstream product

33771-47-0Relevant articles and documents

UMSETZUNG VON LITHIIERTEM 2-HYDROXYBIPHENYL BZW. 2'-HYDROXY-M-TERPHENYL MIT HALOGENVERBINDUNGEN VON SILICIUM UND GERMANIUM, PHOSPHOR UND ARSEN

Maringgele, Walter,Meller, Anton

, p. 235 - 242 (2007/10/02)

The reaction of lithiated 2-hydroxybiphenyl and 2'-hydroxy-m-terphenyl resp. with SiCl4 and SiBr4 resp. yields the aryloxyhalogenosilanes 1-6 and the 1-oxa-10-silaphenanthrenederivative 7.PCl3 and POCl3 resp. react to yield the phosphanes 8-11 and the P(V

Use of Functionalized Ethylene Oligomers To Prepare Recoverable, Recyclable Nickel(0) Diene Cyclooligomerization Catalysts

Bergbreiter, David E.,Chandran, Rama

, p. 4754 - 4760 (2007/10/02)

Polyethylene-bound alkyl diaryl and triaryl phosphites that act as ligands for homogeneous nickel (0) butadiene cyclooligomerization catalysts are described.The homogeneous nickel (0) catalysts prepared in the presence of these ligands are shown to have the same product selectivity and reactivity as similar nickel catalysts prepared from low molecular weight phosphite ligands in reactions carried out at 100 deg C.By varying the ligand/nickel ratio, it is possible to vary the product selectivity of these polyethylene-bound nickel(0) catalysts.High product selectivities (>90percent) for 1,5-cyclooctadiene are attainable.These ethylene oligomer ligated nickel(0) catalysts take advantage of the temperature-dependent solubility properties of polyethylene in order to maintain catalyst homogeneity at 100 deg C during the oligomerization.Recovery and recycling of the catalyst is possible because the catalyst and polyethylene quantitatively coprecipitate on cooling the reaction mixture to 25 deg C.

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