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Benzoic acid, 3-hydroxy-5-(phenylmethoxy)-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

497069-12-2

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497069-12-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 497069-12-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,7,0,6 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 497069-12:
(8*4)+(7*9)+(6*7)+(5*0)+(4*6)+(3*9)+(2*1)+(1*2)=192
192 % 10 = 2
So 497069-12-2 is a valid CAS Registry Number.

497069-12-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 3-hydroxy-5-phenylmethoxybenzoate

1.2 Other means of identification

Product number -
Other names ethyl-3-benzyloxy-5-hydroxy-benzoate

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:497069-12-2 SDS

497069-12-2Downstream Products

497069-12-2Relevant academic research and scientific papers

BENZOATE COMPOUND

-

, (2022/01/04)

The present invention provides a benzoic acid ester compound that has an enteropeptidase inhibitory effect, and use of the compound as a medicament for the treatment or prevention of obesity, diabetes mellitus, or the like. A compound represented by the formula (I) or a salt thereof has an enteropeptidase inhibitory effect and is useful as a medicament for the treatment or prevention of obesity, diabetes mellitus, or the like: [in the formula, each symbol is as defined in the specification].

FUSED HETEROCYCLIC COMPOUND

-

Paragraph 0461-0462, (2018/04/12)

The present invention relates to a condensed heterocyclic compound that has an enteropeptidase inhibitory effect, and use of the compound as a medicament for the treatment or prevention of obesity, diabetes mellitus, or the like. Specifically, the present

Synthesis of organometallic poly(dendrimer)s by macromonomer polymerization: effect of dendrimer size and structural rigidity on the polymerization efficiency

Cheung, Siu-Yin,Chow, Hak-Fun,Ngai, To,Wei, Xiaoling

supporting information; experimental part, p. 2278 - 2288 (2009/10/23)

Two series of first to third generation (G1-G3) oligoether dendrimers, one hearing a shorter spacer chain (C-O) and the other having a longer spacer branch (C-C-C-O) were prepared. Both series of compounds, containing two reactive C≡CH moieties on the dendrimer surface, were used as macromonomers and copolymerized with trans-[Pt(PEt3)2Cl2] to form organometallic poly(dendrimer)s by an outer-sphere-outer-sphere connection strategy. It was found that concentration of monomer used in the polymerization, the dendrimer generation, and, most strikingly, the length of the spacer were key factors that determined the polymerization efficiency. Hence, the structurally more rigid and compact C-O linked dendrimers formed poly(dendrimer)s with a higher degree of polymerization than the structurally less rigid and more bulky C-C-C-O dendrimers. This result was due to the higher tendency to form cyclic oligomers in the latter series of compounds. In addition, the differences in the polymerization efficiency among the three generations of dendrimers could be explained by the gradual decrease of reactive functional group density on the dendrimer surface.

Invertible amphiphilic polymers

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Page/Page column 6; 7, (2010/11/29)

Amphiphilic monomeric compounds and corresponding homopolymers and copolymers capable of assembly and invertible configuration in introduction to and change in fluid medium.

Comparison of facially amphiphilic biaryl dendrimers with classical amphiphilic ones using protein surface recognition as the tool

Klaikherd, Akamol,Sandanaraj, Britto S.,Vutukuri, Dharma Rao,Thayumanavan

, p. 9231 - 9237 (2007/10/03)

Facially amphiphilic biaryl dendrimers are compared with the more classical benzyl ether amphiphilic dendrimers for molecular recognition, using protein binding as the probe. The protein used for the proposed study is chymotrypsin (ChT). A generation-depe

Homopolymer micelles in heterogeneous solvent mixtures

Basu, Subhadeep,Vutukuri, Dharma Rao,Thayumanavan

, p. 16794 - 16795 (2007/10/03)

Amphiphilic homopolymers containing a hydrophilic and a hydrophobic functionality in each monomer unit have been shown to form polar or apolar containers depending on the solvent environment. When presented with a mixture of solvents, these polymeric cont

Invertible amphiphilic homopolymers

Basu, Subhadeep,Vutukuri, Dharma Rao,Shyamroy, Subarana,Sandanaraj, Britto S.,Thayumanavan

, p. 9890 - 9891 (2007/10/03)

Stimuli-responsive polymers and assemblies are viable candidates for the so-called "smart" materials. In this communication, we report a new class of amphiphilic homopolymers that forms micelle-like structures in polar solvents and inverted micelle-like structures in apolar solvents. We demonstrate that these superstructures are the result of the changes in the molecular-level conformations in the monomer. Copyright

A mild deprotection strategy for allyl-protecting groups and its implications in sequence specific dendrimer synthesis

Vutukuri, Dharma Rao,Bharathi, Pandi,Yu, Zhouying,Rajasekaran, Karthik,Tran, My-Huyen,Thayumanavan

, p. 1146 - 1149 (2007/10/03)

A mild deprotection strategy for allyl ethers under basic conditions in the presence of a palladium catalyst is described. Under these conditions, aryl allyl ethers can be cleaved selectively in the presence of alkyl allyl ethers. These conditions are also effective in the deprotection of allyloxycarbonyl groups. The utility of the current methodology in sequence specific dendrimer synthesis is demonstrated.

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