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106456-81-9

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106456-81-9 Usage

Uses

meso-Tetra[4-(allyloxy)phenyl]porphine can be used to chelate copper from wastewater.

Check Digit Verification of cas no

The CAS Registry Mumber 106456-81-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,4,5 and 6 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 106456-81:
(8*1)+(7*0)+(6*6)+(5*4)+(4*5)+(3*6)+(2*8)+(1*1)=119
119 % 10 = 9
So 106456-81-9 is a valid CAS Registry Number.

106456-81-9SDS

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 5,10,15,20-tetrakis(4-prop-2-enoxyphenyl)-21,22-dihydroporphyrin

1.2 Other means of identification

Product number -
Other names -

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:106456-81-9 SDS

106456-81-9Relevant articles and documents

High-Boron-Content Porphyrin-Cored Aryl Ether Dendrimers: Controlled Synthesis, Characterization, and Photophysical Properties

Cabrera-González, Justo,Xochitiotzi-Flores, Elba,Vi?as, Clara,Teixidor, Francesc,García-Ortega, Héctor,Farfán, Norberto,Santillan, Rosa,Parella, Teodor,Nú?ez, Rosario

, p. 5021 - 5031 (2015)

The synthesis and characterization of a set of poly(aryl ether) dendrimers with tetraphenylporphyrin as the core and 4, 8, 16, or 32 closo-carborane clusters are described. A regioselective hydrosilylation reaction on the allyl-terminated functions with c

Rothemund and Adler-Longo Reactions Revisited: Synthesis of Tetraphenylporphyrins under Equilibrium Conditions

Lindsey, Jonathan S.,Schreiman, Irwin C.,Hsu, Henry C.,Kearney, Patrick C.,Marguerettaz, Anne M.

, p. 827 - 836 (2007/10/02)

We present a new synthetic strategy for preparing tetraphenylporphyrins that should greatly expand synthetic entries into porphyrin containing model systems.Pyrrole and the desired benzaldehyde react reversibly at room temperature with trace acid catalysis to form the cyclic tetraphenylporphyrinogen at thermodynamic equilibrium.An oxidant is then added to irreversibly convert the porphyrinogen to the porphyrin.The greater stability of the cyclic porphyrinogen over the open-chain polypyrrylmethanes occurs when the reaction is performed at moderate dilution (10-2 M).The reaction at high dilution or high concentration affords a negligible yield of the cyclic porphyrinogen.Porphyrinogen exchange reactions provide proof of equilibrium.This methodology is complementary to the Adler-Longo procedure, allowing small quantities of porphyrins to be prepared from sensitive aldehydes in 30-40percent yield without difficult purification problems.This methodology is also extended to the preparation of meso-tetraalkylporphyrins and one hybrid porphyrin containing both aryl and alkyl substituents.The mild reaction conditions and convenience of this method permit consideration of new design strategies in preparing complex porphyrins.

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