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156991-90-1

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156991-90-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 156991-90-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,9,9 and 1 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 156991-90:
(8*1)+(7*5)+(6*6)+(5*9)+(4*9)+(3*1)+(2*9)+(1*0)=181
181 % 10 = 1
So 156991-90-1 is a valid CAS Registry Number.

156991-90-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-dichloro-N,N-dipropyl-1,8-naphthyridine-3-carboxamide

1.2 Other means of identification

Product number -
Other names 1,8-Naphthyridine-3-carboxamide,2,4-dichloro-N,N-dipropyl

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:156991-90-1 SDS

156991-90-1Relevant articles and documents

1,8-Naphthyridines II. 2,4-disubstituted N,N-dialkyl-1,8-naphthyridine - 3-carboxamides with anti-inflammatory and/or antiaggressive activities

Di Braccio,Roma,Ghia,Mattioli

, p. 25 - 32 (2007/10/02)

The preparation of the novel N,N-dialkyl-2,4-dichloro-1,8-naphthyridine- 3-carboxamides 1c,e and N,N-dialkyl-2-(alkylamino or cycloalkylamino)-4- chloro-1,8-naphthyridine-3-carboxamides 2b,d-g,j-p is described. These compounds and the previously obtained analogs 1a,b,d,f and 2a,c,h,i have been tested for their anti-inflammatory and antiaggressive activities, as well as for their gross behavioral effects and acute toxicity. Nine of the twenty- two tested compounds exhibited a statistically significant anti-inflammatory activity in the carrageenin-induced edema assay in the rat (1e,f and 2h,o were the most active compounds). On the other hand, an interesting antiaggressive activity was displayed by ten compounds in the isolation- induced aggressiveness test in mice (compounds 2d,i,k showed the highest activity). Structure-activity relationships are briefly discussed.

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