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4659-45-4

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4659-45-4 Usage

Chemical Properties

Clear slightly yellow liquid

Uses

Different sources of media describe the Uses of 4659-45-4 differently. You can refer to the following data:
1. 2,6-Dichlorobenzoyl chloride acts as an important intermediate in organic synthesis, pharmaceuticals, agrochemicals and dyestuffs. It is employed in the substrate activity screening method for the rapid development of novel substrates and their conversion into non-peptidic inhibitors of Cys and Ser proteases. It is also used in the preparation of 1-acyliridoles and (-)-aspicilin. In addition to this, it undergoes esterification of (fluoren-9-ylmethoxy)carbonyl (Fmoc)-amino acids to 4-alkoxybenzyl alcohol polystyrene.
2. 2,6-Dichlorobenzoyl chloride was used:in substrate activity screening method for the rapid development of novel substrates and their conversion into non-peptidic inhibitors of Cys and Ser proteasesin the synthesis of 1-acyliridolesin enantiocontrolled total synthesis of (-)-aspicilin

General Description

2,6-Dichlorobenzoyl chloride participates in esterification of (fluoren-9-ylmethoxy)carbonyl (Fmoc)-amino acids to 4-alkoxybenzyl alcohol polystyrene.

Purification Methods

Reflux the acid chloride for 2hours with excess of acetyl chloride (3 volumes), distil off AcCl followed by the benzoyl chloride. Store it away from moisture. It is an IRRITANT.[Beilstein 9 III 1377.]

Check Digit Verification of cas no

The CAS Registry Mumber 4659-45-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,5 and 9 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4659-45:
(6*4)+(5*6)+(4*5)+(3*9)+(2*4)+(1*5)=114
114 % 10 = 4
So 4659-45-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H3Cl3O/c8-4-2-1-3-5(9)6(4)7(10)11/h1-3H

4659-45-4 Well-known Company Product Price

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  • Aldrich

  • (187518)  2,6-Dichlorobenzoylchloride  99%

  • 4659-45-4

  • 187518-10G

  • 360.36CNY

  • Detail
  • Aldrich

  • (187518)  2,6-Dichlorobenzoylchloride  99%

  • 4659-45-4

  • 187518-50G

  • 1,223.59CNY

  • Detail

4659-45-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-Dichlorobenzoyl chloride

1.2 Other means of identification

Product number -
Other names 2,6-dichloro-benzoyl chloride

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:4659-45-4 SDS

4659-45-4Relevant articles and documents

Ligand-Based Design of Allosteric Retinoic Acid Receptor-Related Orphan Receptor γt (RORγt) Inverse Agonists

Meijer, Femke A.,Doveston, Richard G.,De Vries, Rens M.J.M.,Vos, Ga?l M.,Vos, Alex A.A.,Leysen, Seppe,Scheepstra, Marcel,Ottmann, Christian,Milroy, Lech-Gustav,Brunsveld, Luc

, p. 241 - 259 (2020)

Retinoic acid receptor-related orphan receptor γt (RORγt) is a nuclear receptor associated with the pathogenesis of autoimmune diseases. Allosteric inhibition of RORγt is conceptually new, unique for this specific nuclear receptor, and offers advantages over traditional orthosteric inhibition. Here, we report a highly efficient in silico-guided approach that led to the discovery of novel allosteric RORγt inverse agonists with a distinct isoxazole chemotype. The the most potent compound, 25 (FM26), displayed submicromolar inhibition in a coactivator recruitment assay and effectively reduced IL-17a mRNA production in EL4 cells, a marker of RORγt activity. The projected allosteric mode of action of 25 was confirmed by biochemical experiments and cocrystallization with the RORγt ligand binding domain. The isoxazole compounds have promising pharmacokinetic properties comparable to other allosteric ligands but with a more diverse chemotype. The efficient ligand-based design approach adopted demonstrates its versatility in generating chemical diversity for allosteric targeting of RORγt.

Synthesis of quinazolin-4(1 H)-ones via amination and annulation of amidines and benzamides

Hu, Fangpeng,Cui, Xinfeng,Ban, Zihui,Lu, Guoqiang,Luo, Nan,Huang, Guosheng

supporting information, p. 2356 - 2360 (2019/03/06)

Quinazolinones have broad applications in the biological, pharmaceutical and material fields. Studies on the synthesis of these compounds are therefore widely conducted. Herein, a novel and highly efficient copper-mediated tandem C(sp2)-H amination and annulation of benzamides and amidines for the synthesis of quinazolin-4(1H)-ones is proposed. This synthetic route can be useful for the construction of quinazolin-4(1H)-one frameworks.

N-ACYL AMINO ACID COMPOUNDS AND METHODS OF USE

-

Paragraph 0430; 0431, (2018/03/28)

The invention relates to compounds of formula (I), or a salt thereof wherein R1, A, L, and R2 and n are as described herein. Compounds of formula (I) and pharmaceutical compositions thereof are ανβ1 integrin inhibitors that are useful for treating tissue specific fibrosis.

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