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7438-18-8

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7438-18-8 Usage

General Description

2,4-Dimethoxybenzenediazonium tetrafluoroborate is a chemical compound with the molecular formula C8H10F4N2O2. It is a derivative of the benzene diazonium cation and contains two methoxy groups and four fluorine atoms. 2,4-Dimethoxybenzenediazonium tetrafluoroborate is commonly used as a diazo component in organic synthesis, particularly in the production of azo dyes. It is also used as a reagent in the preparation of various organic compounds and can participate in reactions such as Sandmeyer and Gomberg-Bachmann. 2,4-Dimethoxybenzenediazonium tetrafluoroborate is a potentially hazardous compound and should be handled with care in a laboratory setting.

Check Digit Verification of cas no

The CAS Registry Mumber 7438-18-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,3 and 8 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7438-18:
(6*7)+(5*4)+(4*3)+(3*8)+(2*1)+(1*8)=108
108 % 10 = 8
So 7438-18-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H9N2O2.BF4/c1-11-6-3-4-7(10-9)8(5-6)12-2;2-1(3,4)5/h3-5H,1-2H3;/q+1;-1

7438-18-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-dimethoxybenzenediazonium,tetrafluoroborate

1.2 Other means of identification

Product number -
Other names 2,4-Dimethoxybenzol-diazonium-tetrafluoroborat

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:7438-18-8 SDS

7438-18-8Upstream product

7438-18-8Relevant articles and documents

Palladium catalyzed stereocontrolled synthesis of C-aryl glycosides using glycals and arenediazonium salts at room temperature

Singh, Adesh Kumar,Kandasamy, Jeyakumar

supporting information, p. 5107 - 5112 (2018/07/29)

A stereocontrolled synthesis of aryl-C-glycosides was achieved using glycals and aryldiazonium salts in the presence of palladium acetate. A wide range of glycals including d-glucal, d-galactal, l-rhamnal, d-xylal and d-ribal underwent C-arylation at the anomeric carbon in the presence of different aryldiazonium tetrafluoroborates and gave synthetically useful 2,3-deoxy-3-keto-α-aryl-C-glycosides in good to excellent yields. Broad substrate scope, simple operation and room temperature reactions make this protocol very attractive in organic synthesis.

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