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88920-24-5

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88920-24-5 Usage

General Description

(4-Methoxybenzyloxy)acetic acid is a chemical compound that consists of a benzene ring with a methoxy group attached to it, along with a carboxylic acid group. It is often used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. (4-Methoxybenzyloxy)acetic acid may have potential applications in the development of new drugs due to its ability to act as a building block for more complex molecules. Additionally, it has been studied for its potential biological activity and its role in various chemical reactions. Overall, (4-Methoxybenzyloxy)acetic acid represents an important intermediate in organic chemistry with potential implications for medicinal and agricultural purposes.

Check Digit Verification of cas no

The CAS Registry Mumber 88920-24-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,9,2 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 88920-24:
(7*8)+(6*8)+(5*9)+(4*2)+(3*0)+(2*2)+(1*4)=165
165 % 10 = 5
So 88920-24-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O4/c1-13-9-4-2-8(3-5-9)6-14-7-10(11)12/h2-5H,6-7H2,1H3,(H,11,12)

88920-24-5SDS

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 2-((4-Methoxybenzyl)oxy)acetic acid

1.2 Other means of identification

Product number -
Other names 2-[(4-methoxyphenyl)methoxy]acetic acid

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:88920-24-5 SDS

88920-24-5Relevant articles and documents

Synthesis of a new lactenediyne scaffold equipped with three handles

Banfi, Luca,Guanti, Giuseppe

, p. 7427 - 7429 (2002)

A new lactenediyne scaffold endowed with three attachment points for substituents (handles) was synthesized. This scaffold was designed in order to be used to prepare libraries of compounds possessing a tethered nucleophile, an activating substituent, and DNA-complexing substructures.

An RCM-Based Total Synthesis of the Antibiotic Disciformycin B

Altmann, Karl-Heinz,Waser, Philipp

supporting information, p. 17393 - 17397 (2020/08/14)

The total synthesis of the potent new antibiotic disciformycin B (2) is described, which shows significant activity against methicillin- and vancomycin-resistant Staphylococcus aureus (MRSA/VRSA) strains. The synthetic route is based on macrocyclization o

Discovery of 1,4-Benzodiazepine-2,5-dione (BZD) Derivatives as Dual Nucleotide Binding Oligomerization Domain Containing 1/2 (NOD1/NOD2) Antagonists Sensitizing Paclitaxel (PTX) to Suppress Lewis Lung Carcinoma (LLC) Growth in Vivo

Wang, Suhua,Yang, Jingshu,Li, Xueyuan,Liu, Zijie,Wu, Youzhen,Si, Guangxu,Tao, Yiran,Zhao, Nan,Hu, Xiao,Ma, Yao,Liu, Gang

supporting information, p. 5162 - 5192 (2017/06/28)

Nucleotide-binding oligomerization domain-like receptors (NLRs) are intracellular sensors of pathogen-Associated molecular patterns (PAMPs) and damage-Associated molecular patterns (DAMPs). Previously, we reported nucleotide-binding oligomerization domain-containing protein 1 (NOD1) antagonists (11, 12) and a NOD2 antagonist (9) that sensitized docetaxel (DTX) or paclitaxel (PTX) treatment for breast or lung cancer. In this article, we describe for the first time a 1,4-benzodiazepine-2,5-dione (BZD) derivative (26bh) that acts as a dual NOD1/NOD2 antagonist and inhibits both nuclear factor B (NF-B) and mitogen-Activated protein kinase (MAPK) inflammatory signaling, thereby sensitizing PTX to suppress Lewis lung carcinoma (LLC) growth. After investigation of the compound's cytotoxicity, a systematic structure-Activity relationship (SAR) was completed and revealed several key factors that were necessary to maintain antagonistic ability. This study establishes the possibility for using adjuvant treatment to combat cancer by antagonizing both NOD1 and NOD2 signaling.

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