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DiMethyl 5-ChloroMethyl-1,3-Benzene-Dicarboxylate is a chemical compound with the molecular formula C11H11ClO4. It is a diester of chloromethyl phthalic acid and is known for its potential applications in the production of active pharmaceutical ingredients and as a building block in organic synthesis.

252210-01-8

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252210-01-8 Usage

Uses

Used in Pharmaceutical Industry:
DiMethyl 5-ChloroMethyl-1,3-Benzene-Dicarboxylate is used as an intermediate in the synthesis of pharmaceuticals for its potential to produce active pharmaceutical ingredients.
Used in Agrochemical Industry:
DiMethyl 5-ChloroMethyl-1,3-Benzene-Dicarboxylate is used as an intermediate in the synthesis of agrochemicals, contributing to the development of effective agricultural products.
Used in Organic Synthesis:
DiMethyl 5-ChloroMethyl-1,3-Benzene-Dicarboxylate serves as a building block in organic synthesis, enabling the creation of various chemical compounds.
Used in Biocatalysis:
DiMethyl 5-ChloroMethyl-1,3-Benzene-Dicarboxylate is identified as a potential substrate for enzyme-catalyzed reactions, making it a valuable tool in the field of biocatalysis for enhancing chemical and pharmaceutical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 252210-01-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,2,2,1 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 252210-01:
(8*2)+(7*5)+(6*2)+(5*2)+(4*1)+(3*0)+(2*0)+(1*1)=78
78 % 10 = 8
So 252210-01-8 is a valid CAS Registry Number.

252210-01-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl 5-(chloromethyl)benzene-1,3-dicarboxylate

1.2 Other means of identification

Product number -
Other names Dimethyl5-Chloromethyl-1,3-Benzene-Dicarboxylate

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:252210-01-8 SDS

252210-01-8Relevant academic research and scientific papers

BIVALENT TARGETED CONJUGATES

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Page/Page column 59; 60, (2020/05/28)

The invention provides conjugates that comprise a bivalent targeting moiety, a nucleic acid, and optional linking groups as well as synthetic intermediates and synthetic methods useful for preparing the conjugates, compositions comprising the bidentate targeting ligands and the conjugates, as well as methods for targeting therapeutic nucleic acids with the bidentate conjugates. The conjugates are useful to target therapeutic nucleic acids.

THERAPEUTIC METHODS

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Page/Page column 204; 231-232, (2020/05/28)

The invention provides methods and compositions for delivering a nucleic acid to a cell or the cytosol of the target cell. The method includes contacting the cell with, 1) a membrane-destabilizing polymer; and 2) a nucleic acid conjugate. The nucleic acid conjugate includes a targeting ligand bound to an optional linker and a nucleic acid.

Radiolabeled Dibenzodiazepinone-Type Antagonists Give Evidence of Dualsteric Binding at the M2 Muscarinic Acetylcholine Receptor

Pegoli, Andrea,She, Xueke,Wifling, David,Hübner, Harald,Bernhardt, Günther,Gmeiner, Peter,Keller, Max

supporting information, p. 3314 - 3334 (2017/05/05)

The dualsteric ligand approach, aiming at ligands with improved subtype selectivity, has been increasingly applied to muscarinic receptors (MRs). In this article, we present the synthesis and characterization of a M2R subtype-preferring radiola

Hybrid materials based on novel 2D lanthanide coordination polymers covalently bonded to amine-modified SBA-15 and MCM-41: assembly, characterization, structural features, thermal and luminescence properties

Wang, Jun,Dou, Wei,Kirillov, Alexander M.,Liu, Weisheng,Xu, Cailing,Fang, Ran,Yang, Lizi

supporting information, p. 18610 - 18621 (2016/12/03)

Three novel 2D coordination polymers [Tb2(μ4-L)2(μ-HL)(μ-HCOO)(DEF)]n (Tb-L), [Eu(μ4-L)(L)(H2O)2]n (Eu-L), and [Nd(μ4-L)(L)(H2O)2]sub

Peptide dendrimers with designer core for directed self-assembly

Verma, Ram P.,Shandilya, Ashutosh,Haridas

supporting information, p. 8758 - 8765 (2015/10/20)

A series of designer peptide dendrimers with urea and urea-triazole cores were synthesized. Urea cored dendrimers assembled into fibrillar morphology, while dendrimers with urea-triazole core assembled into vesicular morphology. The core-dependent self-as

Non-aqueous pigmented inkjet inks

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Page/Page column 29, (2012/03/27)

A non-aqueous inkjet ink includes C.I. Pigment Yellow 150 and a polymeric dispersant according to Formula (I): wherein, T represents hydrogen or a polymerization terminating group; Z represents the residue of polyethyleneimine having a number-average mole

Multi-tier dendrimers with an aromatic core

Haridas,Sharma, Yogesti K.,Naik, Sarala

body text, p. 1570 - 1577 (2009/07/11)

We report various multi-tier designer dendritic molecules that incorporate an aromatic core and heterocyclic and peptide units. The 5-(azidomethyl)benzene- 1,3-dicarbonyl unit was chosen as the scaffold as this unit allows two identical units and a reacti

On the meaning of affinity: Cluster glycoside effects and concanavalin a

Dimick, Sarah M.,Powell, Steven C.,McMahon, Stephen A.,Moothoo, Davina N.,Naismith, James H.,Toone, Eric J.

, p. 10286 - 10296 (2007/10/03)

The inhibition of protein - carbohydrate interaction provides a powerful therapeutic strategy for the treatment of myriad human diseases. To date, application of such approaches have been frustrated by the inherent low affinity of carbohydrate ligands for

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