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4-METHOXY-3-METHOXYMETHYL-BENZALDEHYDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

76646-41-8

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76646-41-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76646-41-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,6,4 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 76646-41:
(7*7)+(6*6)+(5*6)+(4*4)+(3*6)+(2*4)+(1*1)=158
158 % 10 = 8
So 76646-41-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O3/c1-12-7-9-5-8(6-11)3-4-10(9)13-2/h3-6H,7H2,1-2H3

76646-41-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methoxy-3-(methoxymethyl)benzaldehyde

1.2 Other means of identification

Product number -
Other names 4-Methoxy-3-methoxymethyl-benzaldehyde

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:76646-41-8 SDS

76646-41-8Relevant academic research and scientific papers

ANTI-FIBROTIC COMPOUNDS

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Paragraph 00352; 00359, (2018/08/26)

Provided herein are anti-fibrotic compounds, in particular those of Formula (I), that inhibit the TGF-beta signaling pathway. Also provided are pharmaceutical compositions comprising the anti-fibrotic compounds, and methods of treating diseases or conditions associated with fibrosis, inflammation, and benign or malignant neoplastic diseases in a subject by administering a compound or composition described herein. (Formula (I))

Synthetic Study of Selective Benzylic Oxidation

Wang, Wuyi,Li, Tiechao,Attardo, Giorgio

, p. 6598 - 6602 (2007/10/03)

Oxidation of bisbenzyl ethers was studied using 2,3-dichloro-5,6-dicyanobenzoquinone (DDQ). Compared to other benzylic oxidations such as Kornblum type reaction of benzyl bromides or MnO2 oxidation of benzyl alcohols, DDQ oxidation offered advantages of being mild and highly selective to provide monoaldehyde products. We have explored factors which influence the course of the reaction and exemplified the synthetic value of the approach by preparing a number of aromatic intermediates (7-8, 15-25).

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