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6-chloro-2,3-dihydro-4H-pyrano<2,3-b>pyridin-4-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

122433-49-2

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122433-49-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 122433-49-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,4,3 and 3 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 122433-49:
(8*1)+(7*2)+(6*2)+(5*4)+(4*3)+(3*3)+(2*4)+(1*9)=92
92 % 10 = 2
So 122433-49-2 is a valid CAS Registry Number.

122433-49-2SDS

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 6-chloro-2,3-dihydropyrano[2,3-b]pyridin-4-one

1.2 Other means of identification

Product number -
Other names 6-CHLORO-2H-PYRANO[2,3-B]PYRIDIN-4(3H)-ONE

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:122433-49-2 SDS

122433-49-2Downstream Products

122433-49-2Relevant academic research and scientific papers

Spiro hydantoin aldose reductase inhibitors derived from 8-aza-4-chromanones

Sarges,Goldstein,Welch,Swindell,Siegel,Beyer

, p. 1859 - 1865 (2007/10/02)

A series of spiro hydantoins derived from 8-azachromanones (2,3-dihydro-4H-pyrano[2,3-b]pyridin-4-ones) has been prepared and tested for aldose reductase inhibitory activity. The standard Bucherer-Bergs conditions had to be drastically modified to increas

Azolidinedione derivatives

-

, (2008/06/13)

A series of novel spiro-deteroazolones derived from a 2,3-dihydropryrano[2,3-b]pyridine ring system have been prepared, including their pharmaceutically acceptable salts. These compounds are useful in therapy as aldose reductase inhibitors for the control of certain chronic diabetic complications. Typical member compounds include spiro-imides, spiro-oxazolidinediones, spiro-thiazolidinediones and spiro-imidazolidinediones derived from the aforesaid ring system. (4'S) (2'R)-6'-Chloro-2',3'-dihydro-2'-methyl-spiro-[imidazolidine-4,4'-4'H-pyrano[2,3-b]pyridine]-2,5-dione represents a typical and preferred member compound. Methods for preparing all these compounds from known starting materials are provided.

Azolidinedione derivatives

-

, (2014/02/10)

Spiro-heteroazolones of formula wherein, Z is methylene, oxygen, sulfur or imino; Y is oxygen or sulfur; and -A=B-D=E- represents -N=CH-CH=CH-, -CH=N-CH=CH-, -CH=CH-N=CH or -CH=CH-CH=N-, or an N-oxide derivative thereof. These compounds are useful in therapy as aldose reductase inhibitors for the control of certain chronic diabetic complications. Typical member compounds include spiro-imides, spiro-oxa-zolidinediones, spiro-thiazolidinediones and spiro-imidazolidinediones derived from the aforesaid ring system. (4'S)(2'R)-6'-Chloro-2',3'-dihydro-2'-methyl--spiro-[imidazolidine-4,4'-4'H-pyrano[2,3-b]pyridine]--2,5-dione represents a typical and preferred member compound. Methods for preparing all these compounds from known starting materials are provided.

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