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Phosphonium, (2,4-dimethoxy-4-oxo-2-butenyl)triphenyl-, bromide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

71575-67-2

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71575-67-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71575-67-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,5,7 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 71575-67:
(7*7)+(6*1)+(5*5)+(4*7)+(3*5)+(2*6)+(1*7)=142
142 % 10 = 2
So 71575-67-2 is a valid CAS Registry Number.

71575-67-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,4-dimethoxy-4-oxobut-2-enyl)-triphenylphosphanium,bromide

1.2 Other means of identification

Product number -
Other names Phosphonium,(2,4-dimethoxy-4-oxo-2-butenyl)triphenyl-,bromide

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:71575-67-2 SDS

71575-67-2Relevant articles and documents

Multifunctional Cyclopentadienes as a Scaffold for Combinatorial Bioorganometallics in [(η5-C5H2R1R2R3)M(CO)3] (M=Re, 99mTc) Piano-Stool Complexes

Frei, Angelo,Spingler, Bernhard,Alberto, Roger

, p. 10156 - 10164 (2018/07/29)

Multifunctional cyclopentadiene (Cp) ligands and their rhenium and 99mTc complexes were prepared by a versatile synthetic route. The properties of these Cp ligands can be tuned on demand, either during their synthesis (variation of R1) or through post-synthetic functionalization with two equal or different vectors (V1 and V2). Variation of these groups enables a combinatorial approach in the synthesis of bioorganometallic complexes. This is demonstrated by the preparation of Cp ligands containing both electron-donating and electron-withdrawing groups at the R1 position and their subsequent homo- or heterofunctionalization with biovector models (benzylamine and phenylalanine) under standard amide bond-formation conditions. All ligands can be coordinated to the fac-[Re(CO)3]+ and fac-[99mTc(CO)3]+ cores to give tetrafunctional complexes in straightforward and functional-group-tolerant procedures. The 99mTc complexes were prepared in one step, in 30 min, and under aqueous conditions from generator-eluted [99mTcO4]?.

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