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252210-01-8

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252210-01-8 Usage

General Description

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 commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. DiMethyl 5-ChloroMethyl-1,3-Benzene-Dicarboxylate is known for its potential applications in the production of active pharmaceutical ingredients and is often used as a building block in organic synthesis. Additionally, it has been identified as a potential substrate for enzyme-catalyzed reactions, making it a valuable tool in the field of biocatalysis. Due to its unique chemical structure, DiMethyl 5-ChloroMethyl-1,3-Benzene-Dicarboxylate has the potential to be used in a wide range of 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 articles and documents

BIVALENT TARGETED CONJUGATES

-

, (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.

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

, 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

Peptide dendrimers with designer core for directed self-assembly

Verma, Ram P.,Shandilya, Ashutosh,Haridas

, 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

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