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118888-62-3

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118888-62-3 Usage

General Description

3-Methoxyphenylglyoxal hydrate is a chemical compound with the molecular formula C9H10O4. It is a hydrate of 3-methoxyphenylglyoxal, which is an aromatic aldehyde. 3-METHOXYPHENYLGLYOXAL HYDRATE is used in the synthesis of various pharmaceuticals and natural products. It is also used as a reagent in organic chemistry reactions, particularly in the formation of carbon-carbon and carbon-nitrogen bonds. 3-Methoxyphenylglyoxal hydrate has potential applications in the development of new drugs and medicinal compounds due to its unique chemical properties.

Check Digit Verification of cas no

The CAS Registry Mumber 118888-62-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,8,8 and 8 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 118888-62:
(8*1)+(7*1)+(6*8)+(5*8)+(4*8)+(3*8)+(2*6)+(1*2)=173
173 % 10 = 3
So 118888-62-3 is a valid CAS Registry Number.

118888-62-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-methoxyphenyl)-2-oxoacetaldehyde,hydrate

1.2 Other means of identification

Product number -
Other names OR1626

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:118888-62-3 SDS

118888-62-3Upstream product

118888-62-3Relevant articles and documents

Regioselective N-1 and C-2 diacylation of 3-substituted indoles with arylglyoxal hydrates for the synthesis of indolyl diketones

Pan, Dalong,Chu, Jinpeng,Gao, Xianrui,Wang, Cuiping,Meng, Qingtao,Chi, Haijun,Dong, Yan,Duan, Chunying,Zhang, Zhiqiang

supporting information, p. 6998 - 7003 (2018/10/17)

A highly regioselective N-1 and C-2 diacylation of 3-substituted indoles with arylglyoxal hydrates to afford N-1 and C-2 indolyl diketones in moderate to good yields is described. Notably, the control of regioselectivity is achieved by small changes in the Cu catalyst, additive and solvent. Importantly, the intermediates for N-1 and C-2 diacylation were detected and two plausible pathways were also proposed.

Synthesis and antitumor evaluation of 2,3-diarylbenzofuran derivatives on HeLa cells

He, Guo-Xue,Yuan, Jing-Mei,Zhu, Hai-Miao,Wei, Kai,Wang, Ling-Yun,Kong, Shi-Lin,Mo, Dong-Liang,Pan, Cheng-Xue,Su, Gui-Fa

supporting information, p. 1660 - 1664 (2017/04/04)

2,2-Dihydroxyarylethanones, readily prepared from the commercially available aromatic ethyl ketones, were reacted with resorcinol, 3-methoxyphenol or 2-methoxyphenol in multi steps one-pot manner promoted by trifluoroacetic acid to furnish the 2,3-diarylbenzofuran derivatives in 22–95% yield. Sixteen targeted compounds were synthesized and characterized by 1H NMR, 13C NMR and HRMS. MTT assay indicated that most compounds possessed effectively inhibitory activities against the proliferation of HeLa cell. Among them, 4f had the highest inhibitory activities, with the IC50 being 13.40?±?2.04?μmol/L. Cell cycle analysis, Annexin V-FITC/propidium iodide dual staining assay and western blotting analysis revealed that 4f inhibited the proliferation of Hela cell through apoptosis induction in a dose-dependent manner via obviously up-regulated the levels of Bak and Bim, while striking down-regulated the level of Bcl-2 and Bcl-xL protein.

Copper-Assisted Synthesis of 2-Hydroxyphenyl-1,2-diones from Phenols and 2-Oxoaldehydes

Battini, Narsaiah,Battula, Satyanarayana,Ahmed, Qazi Naveed

supporting information, p. 658 - 662 (2017/01/18)

An efficient copper(II)-catalyzed protocol for the ortho-functionalization of phenols was developed. A wide variety of 2-oxoaldehydes and phenols were tolerated, and the corresponding 2-hydroxyphenyl-1,2-diones were afforded in appreciable yields.

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