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15450-80-3

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15450-80-3 Usage

Type of compound

Phosphole oxide

Heteroatoms in the ring

Phosphorus and oxygen

Ring structure

Five-membered heterocyclic

Methyl groups

Three (attached to the phosphole ring)

Structure

Highly branched

Application

Commonly used as a ligand in coordination chemistry and organometallic chemistry

Complex formation

Can form stable complexes with transition metals

Unique property

Ability to coordinate with metal ions

Significance

Valuable building block for the synthesis of novel organic and inorganic compounds

Check Digit Verification of cas no

The CAS Registry Mumber 15450-80-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,4,5 and 0 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 15450-80:
(7*1)+(6*5)+(5*4)+(4*5)+(3*0)+(2*8)+(1*0)=93
93 % 10 = 3
So 15450-80-3 is a valid CAS Registry Number.

15450-80-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,4-trimethyl-2,5-dihydro-1λ<sup>5</sup>-phosphole 1-oxide

1.2 Other means of identification

Product number -
Other names 1,3,4-trimethyl-2,5-dihydro-1H-phosphole 1-oxide

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:15450-80-3 SDS

15450-80-3Downstream Products

15450-80-3Relevant articles and documents

The Reaction of 1-Substituted 3,4-Dimethyl-Δ3-phospholens with Diethyl Peroxide: a Correlation Between Rate and 31P Nuclear Magnetic Resonance Shift

Hammond, Philip J.,Scott, Graham,Hall, C. Dennis

, p. 205 - 210 (2007/10/02)

The reactions of a variety of 1-X-3,4-dimethyl-Δ3-phospholens (where X=Br, Me, Ph, NMe2, SEt, H, and OR) with diethyl peroxide are described.The rates of reaction show a broad correlation with the 31P n.m.r. chemical shifts of the starting phospholens, with low field shifts corresponding to the highest reactivity.The results are discussed in terms of the biphilic mechanism for the reaction of trico-ordinate phosphorus compounds with weak ?-bonds.

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