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2-amino-4-chlorophenol-5-sulphonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

41406-65-9

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41406-65-9 Usage

Compound

2-amino-4-chlorophenol-5-sulphonamide

Derived from

sulfonamide

Groups present

amine and sulphonamide group

Main use

antimicrobial agent

Properties

antibacterial

Applications

production of pharmaceuticals, dyes, industrial applications

Function

inhibits growth of bacteria, development of medications for bacterial infections

Check Digit Verification of cas no

The CAS Registry Mumber 41406-65-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,4,0 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 41406-65:
(7*4)+(6*1)+(5*4)+(4*0)+(3*6)+(2*6)+(1*5)=89
89 % 10 = 9
So 41406-65-9 is a valid CAS Registry Number.

41406-65-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-4-chlorophenol-5-sulphonamide

1.2 Other means of identification

Product number -
Other names N-<2-Dimethylamino-ethyl>-4.5.6.7-tetrachlor-isoindolin

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:41406-65-9 SDS

41406-65-9Relevant academic research and scientific papers

Primary amine-functional benzoxazine monomers and their use for amide-containing monomeric benzoxazines

Agag, Tarek,Arza, Carlos R.,Maurer, Frans H. J.,Ishida, Hatsuo

experimental part, p. 2748 - 2758 (2011/10/09)

Amino-functional benzoxazine monomers have been successfully prepared. Several routes have been applied to incorporate amino group into benzoxazine structure. These approaches include reduction of the corresponding nitro-functional benzoxazines and deprot

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