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1878-85-9

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1878-85-9 Usage

Chemical Properties

White powder

Check Digit Verification of cas no

The CAS Registry Mumber 1878-85-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,7 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1878-85:
(6*1)+(5*8)+(4*7)+(3*8)+(2*8)+(1*5)=119
119 % 10 = 9
So 1878-85-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H10O4/c1-12-7-4-2-3-5-8(7)13-6-9(10)11/h2-5H,6H2,1H3,(H,10,11)/p-1

1878-85-9 Well-known Company Product Price

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  • Alfa Aesar

  • (B20672)  2-Methoxyphenoxyacetic acid, 98+%   

  • 1878-85-9

  • 5g

  • 374.0CNY

  • Detail
  • Alfa Aesar

  • (B20672)  2-Methoxyphenoxyacetic acid, 98+%   

  • 1878-85-9

  • 25g

  • 1028.0CNY

  • Detail

1878-85-9SDS

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-(2-methoxyphenoxy)acetic acid

1.2 Other means of identification

Product number -
Other names O-(2-Methoxy-phenyl)-glykolsaeure

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:1878-85-9 SDS

1878-85-9Relevant articles and documents

New Multidentate Compounds of Ether-Ester Type

Lin, Whei Oh,de Souza, Maria C. Bastos Viera,Altoe, Antonio P.,Alt, Helmut G.

, p. 359 - 364 (1983)

A series of ether-esters containing multidentate components have been prepared from phenoxyacetic acid.The ligands were synthesized from the appropriate phenoxyacetic acid chloride and various alcohols.Four types of new compounds have been obtained. - Keywords: Acyclic crown compounds; Ester-ether crown compounds; Multidentate ligands; Phenoxyacetic acid ester

Modulation of DNA damage response by targeting ATM kinase using newly synthesized di-phenoxy acetamide (DPA) analogs to induce anti-neoplasia

Al-Ostoot, Fares Hezam,Sherapura, Ankith,Malojirao, Vikas H.,Thirusangu, Prabhu,Al-Muhimeed, Tahani I.,Khanum, Shaukath Ara,Prabhakar

, p. 1344 - 1360 (2021/06/14)

Background: Imbalance and instability in the structure of the DNA have become major characteristics of cancer. In response to DNA damage, DNA damage response (DDR) protein, ataxia telangiectasia mutated (ATM), plays a pivotal role in the modulation of regulatory regions responsible for inhibition of apoptosis, thereby neoplastic progression. Methods: A new series of DPA (7a–t) were synthesized, characterized. Anti-proliferative studies to identify the lead compound were carried out by LDH and MTT assay. Apoptosis/DNA damage was measured through FACS, Annexin-v staining, TUNEL and Comet assay. Elucidation of molecular mechanism through immunoblot and further validation of the drug effect through in vivo approaches. Results: Initial in vitro anti-proliferative screening of Compounds DPA (7a–t) against multiple cancer cell lines identified Compound DPA (7n) as a potent cytotoxic molecule with IC50 value of 4.3?μM. Down the line, in vitro and in vivo evaluation of Compound DPA (7n) inferred that it has apoptotic inducing potentiality. Further, evaluation of molecular mechanism inferred that Compound DPA (7n) effectively modulates ATM phosphorylation only, eventually altering downstream signalling pathways. Conclusions: Compound DPA (7n) emerged as a potent proapoptotic and anti-neoplastic agent by inhibiting ATM kinase activity both in vitro and in vivo. The conferring results ascertain that the drug could be developed as a new ATM kinase inhibitor with anti-cancer capacity. Graphic abstract: [Figure not available: see fulltext.]

Electrochemical Aminoxyl-Mediated Oxidation of Primary Alcohols in Lignin to Carboxylic Acids: Polymer Modification and Depolymerization

Rafiee, Mohammad,Alherech, Manar,Karlen, Steven D.,Stahl, Shannon S.

supporting information, p. 15266 - 15276 (2019/10/19)

An electrochemical process has been developed for chemoselective oxidation of primary alcohols in lignin to the corresponding carboxylic acids. The electrochemical oxidation reactions proceed under mildly basic conditions and employ 2,2,6,6-tetramethyl-1-piperidine N-oxyl (TEMPO) and 4-acetamidoO (ACT) as catalytic mediators. Lignin model compounds and related alcohols are used to conduct structure-reactivity studies that provide insights into the origin of the reaction selectivity. The method is applied to the oxidation of lignin extracted from poplar wood chips via a mild acidolysis method, and the reaction affords a novel polyelectrolyte material. Gel permeation chromatography data for the oxidized lignin shows that this material has a molecular weight and molecular weight distribution very similar to that of the extracted lignin, but notable differences are also evident. Base titration reveals a significant increase in the acid content, and the oxidized lignin has much higher water solubility relative to the extracted lignin. Treatment of the oxidized lignin under acidic conditions results in depolymerization of the material into characterized aromatic monomers in nearly 30 wt% yield.

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