Welcome to LookChem.com Sign In|Join Free

CAS

  • or

850308-65-5

Post Buying Request

850308-65-5 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

850308-65-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 850308-65-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,0,3,0 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 850308-65:
(8*8)+(7*5)+(6*0)+(5*3)+(4*0)+(3*8)+(2*6)+(1*5)=155
155 % 10 = 5
So 850308-65-5 is a valid CAS Registry Number.

850308-65-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name α-(di-tert-butylphosphino)-α'-(diphenylphosphino)-o-xylene

1.2 Other means of identification

Product number -
Other names α-(di-tert-butylphosphino)-α'-(diphenylphosphino)xylene

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:850308-65-5 SDS

850308-65-5Relevant articles and documents

Synthesis and characterisation of novel o-xylene-based P,E ligands

Allan, Kathryn M.,Spencer, John L.

, p. 956 - 964 (2014/02/14)

A range of novel hybrid ligands of the type, o-C6H 4(CH2PBut2)(CH2E) (E = P(C6F5)2, SBut, SPh, S(O)Bu t, NR2, SiPh2H), have been synthesised in two or three steps from the common substrate, o-C6H4{CH 2PBut2(BH3)}(CH2Cl). The initial step involved treatment of the substrate with the appropriate nucleophilic reagent, or preparation of a Grignard reagent from o-C 6H4{CH2PBut2(BH 3)}(CH2Cl) and reaction with the appropriate electrophile. In most cases, this versatile strategy produced air-stable crystalline ligand precursors. Phosphine deprotection was achieved via one of three methods, dependent upon the properties of the second functional group. An alternative synthesis of the known ligand, o-C6H4(CH 2PBut2)(CH2PPh2), is also presented.

PROCESS FOR THE CARBONYLATION OF ETHYLENICALLY UNSATURATED COMPOUNDS, NOVEL CARBONYLATION LIGANDS AND CATALYST SYSTEMS INCORPORATING SUCH LIGANDS

-

Page/Page column 50-51; 54-55, (2010/04/03)

A novel bidentate catalytic ligand of general formula (I) is described. R represents a hydrocarbyl aromatic structure having at least one aromatic ring to which Q 1 and Q 2 are each linked, via the respective linking group, if present, on available adjacent atoms of the at least one aromatic ring. The groups X 3 and X 4 represent radicals joined via tertiary carbon atoms to the respective atom Q 1 and the groups X 1 and X 2 represent radicals joined via primary, or substituted aromatic ring carbon atom(s) to the respective atom Q 2. A and B represent an optional lower alkylene linking group. Q 1 and Q 2 each represent phosphorus, arsenic or antimony. A process for the carbonylation of ethylenically unsaturated compounds comprising reacting the compound with carbon monoxide in the presence of a source of hydroxyl groups, optionally, a source of anions and catalyst system obtainable by combining a metal of Group 8, 9 or 10 or a compound thereof and the bidentate ligand of general formula (I) is also described.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 850308-65-5