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4-Pyridinesulfonamide,3-amino-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

164406-91-1

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164406-91-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 164406-91-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,4,4,0 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 164406-91:
(8*1)+(7*6)+(6*4)+(5*4)+(4*0)+(3*6)+(2*9)+(1*1)=131
131 % 10 = 1
So 164406-91-1 is a valid CAS Registry Number.

164406-91-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-aminopyridine-4-sulfonamide

1.2 Other means of identification

Product number -
Other names 4-pyridinesulfonamide,3-amino

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:164406-91-1 SDS

164406-91-1Downstream Products

164406-91-1Relevant academic research and scientific papers

FUSED [1,2,4]THIADIAZINE DERIVATIVES WHICH ACT AS KAT INHIBITORS OF THE MYST FAMILY

-

, (2019/03/17)

A compound of formula (I): which inhibits the activity of one or more KATs of the MYST family, i.e., TIP60, KAT6B, MOZ, HBO1 and MOF.

Synthesis of pyrido-1,2,4-thiadiazines related to antihypertensive 1,2,4-benzothiadiazine-1,1-dioxides

Neill, Colin G.,Preston, Peter N.,Wightman, Richard H.

, p. 13645 - 13654 (2007/10/03)

Oxidation of 3-phenyl-2H-pyrido[2,3-e]-1,2,4-thiadiazine with sodium hypochlorite and, separately, m-chloroperoxybenzoic acid afforded a 1,1- dioxide and a 5-oxide derivative, respectively. Further examples of such 1,1- dioxide derivatives were synthesised by treating 2-amino-5-methylpyridine with orthoesters and these were subsequently oxidised to novel 1,1,5- trioxides. A short route has been developed for the synthesis of 4- aminopyridine-3-sulfonamide which was used for the preparation of 4H- pyrido[4,3-e]-1,2,4-thiadiazine 1,1-dioxides; oxidation of the parent member of the series gave a 1,1,7-trioxide derivative. 3-Aminopyridine-4-sulfonamide has been prepared, and then condensed with triethyl orthoformate to afford 4H-pyrido[3,4-e]-1,2,4-thiadiazine 1,1-dioxide.

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