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3,5-Dibromoyridine-4-sulfonic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

872273-27-3

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872273-27-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 872273-27-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,2,2,7 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 872273-27:
(8*8)+(7*7)+(6*2)+(5*2)+(4*7)+(3*3)+(2*2)+(1*7)=183
183 % 10 = 3
So 872273-27-3 is a valid CAS Registry Number.

872273-27-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-dibromopyridine-4-sulfonic acid

1.2 Other means of identification

Product number -
Other names 3,5-dibromo-pyridine-4-sulfonic 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:872273-27-3 SDS

872273-27-3Relevant academic research and scientific papers

Synthetic method of 3, 5-dibromopyridine

-

, (2017/08/31)

The invention discloses a synthetic method of 3, 5-dibromopyridine. The synthetic method comprises the following steps of: (1) bromination reaction: dissolving 4-aminopyridine and azodiisobutyronitrile in carbon tetrachloride; adding N-bromosuccinimide at the temperature of 25 DEG C, carrying out central-control monitoring using a liquid phase till the reaction is complete, and treating to obtain 3, 5-dibromo-4-aminopyridine; (2) diazotization reaction: adding the 3, 5-dibromo-4-aminopyridine into concentrated sulfuric acid, dripping nitrosylsulfuric acid at the temperature of 48-55 DEG C after completely dissolving, stopping dripping when potassium iodide starch test paper is blue and does not fade, and then reacting for 1-1.5 hours; and (3) reduction reaction: continuously adding nickel powder and anhydrous ethanol solution into the solution, then carrying out refluxing reaction, cooling and then adjusting to be weakly alkaline by using concentrated sodium-hydroxide solution, and treating to obtain the 3, 5-dibromopyridine. The synthetic method disclosed by the invention has the advantages that the reaction condition is mild, the yield is high, the materials are easily available, the cost is lower, the process route is short, and the product purity is high and has industrial prospect.

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