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Benzenemethanol, 3,5-bis[[3,5-bis[[3,5-bis(phenylmethoxy)phenyl]methoxy]phenyl]methoxy] - is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

137472-16-3

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137472-16-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 137472-16-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,4,7 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 137472-16:
(8*1)+(7*3)+(6*7)+(5*4)+(4*7)+(3*2)+(2*1)+(1*6)=133
133 % 10 = 3
So 137472-16-3 is a valid CAS Registry Number.

137472-16-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name [3,5-bis[[3,5-bis[[3,5-bis(phenylmethoxy)phenyl]methoxy]phenyl]methoxy]phenyl]methyl alcohol

1.2 Other means of identification

Product number -
Other names {3,5-Bis-[3,5-bis-(3,5-bis-benzyloxy-benzyloxy)-benzyloxy]-phenyl}-methanol

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:137472-16-3 SDS

137472-16-3Relevant academic research and scientific papers

A fast double-stage convergent synthesis of dendritic polyethers

L'abbe, Gerrit,Forier, Bart,Dehaen, Wim

, p. 2143 - 2144 (1996)

Two tert-butyldiphenylsilyl-protected synthons 7 and 9 are prepared in excellent yields and used in a one-pot synthesis of higher generation polyether dendrons.

Synthesis of dendritic phenol ether derivatives with a naphthalene core

Xiang, Zhonghua,Cao, Derong

, p. 1318 - 1324 (2008/09/19)

A series of dendritic phenol ether derivatives with a naphthalene core were synthesized by the Williamson reaction as a coupling reaction between 1-hydroxymethylnaphthalene and polyether-based dendritic fragments in the presence of phase-transfer catalyst and alkali. The modified method for chlorination of dendritic benzyl alcohol was also developed using PPh3 and CCl4 as reagents and CH2Cl2/CCl4 as solvent. Copyright Taylor & Francis Group, LLC.

Optical switching and antenna effect of dendrimers with an anthracene core

Cao, Derong,Dobis, Silvia,Gao, Chunmei,Hillmann, Sabine,Meier, Herbert

, p. 9317 - 9323 (2008/12/20)

Dendrimers 6Gi (i=1-4) consisting of an anthracene core and Frechet dendrons which are attached via a CH2OCH2 chain in the 9-position undergo quantitative and completely reversible intramolecular [4π+4π] cycloaddition. The

Facile synthesis of aryl ether dendrimer from unprotected AB2 building blocks using thionyl chloride as an activating agent

Yamazaki, Natsuko,Washio, Isao,Shibasaki, Yuji,Ueda, Mitsuru

, p. 2321 - 2324 (2007/10/03)

A novel, rapid, inexpensive, and highly efficient convergent approach for the synthesis of a Frechet- type aryl ether dendrimer using thionyl chloride has been developed. In this method, the purification of each dendron and a dendrimer occurs by recrystallization, extraction, and precipitation. The MALDI-TOF MS spectrum supported the formation of the G2, G3, and G4 dendrons and the star-shaped G4 dendrimer.

Photoisomerization of stilbene dendrimers: The need for a volume-conserving isomerization mechanism

Uda, Mayuko,Mizutani, Takuo,Hayakawa, Junpei,Momotake, Atsuya,Ikegami, Masashi,Nagahata, Ritsuko,Arai, Tatsuo

, p. 596 - 605 (2007/10/03)

Highly branched stilbene dendrimers were synthesized and their photochemical behavior was studied. Even the stilbene dendrimer with molecular weight over 6500 underwent transcis isomerization in the excited singlet state within the lifetime of 10 ns. The

Alternative convergent and accelerated double-stage convergent approaches towards functionalized dendritic polyethers

Forier,Dehaen

, p. 9829 - 9846 (2007/10/03)

Alternative convergent synthesis strategies for the preparation of dendritic macromolecules, using either mesylate activation or the Mitsunobu reaction, are described. The synthesis can be further accelerated by using a double stage convergent approach. T

Preparation of polymers with controlled molecular architecture. A new convergent approach to dendritic macromolecules

Hawker, Craig J.,Fréchet

, p. 7638 - 7647 (2007/10/02)

The novel convergent growth approach to topological macromolecules based on dendritic fragments is described. The polyether dendritic fragments are prepared by starting from what will become the periphery of the molecule and progressing inward. In the fir

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