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116247-30-4

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116247-30-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 116247-30-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,2,4 and 7 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 116247-30:
(8*1)+(7*1)+(6*6)+(5*2)+(4*4)+(3*7)+(2*3)+(1*0)=104
104 % 10 = 4
So 116247-30-4 is a valid CAS Registry Number.

116247-30-4SDS

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 4-oxo-7-(trifluoromethyl)-1H-quinoline-3-carbohydrazide

1.2 Other means of identification

Product number -
Other names 7-Trifluoromethyl-4-hydroxyquinoline-3-carboxylic acid hydrazide

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:116247-30-4 SDS

116247-30-4Relevant articles and documents

Synthesis, characterization and antimicrobial studies of some new trifluoromethyl quinoline-3-carbohydrazide and 1,3,4-oxadiazoles

Garudachari,Isloor, Arun M.,Satyanaraya,Ananda,Fun, Hoong-Kun

, p. 30864 - 30875 (2014/08/05)

The present paper describes the synthesis of two new series of 7-(trifluoromethyl)-4-hydroxy substituted quinoline carbohydrazide derivatives (6a-e and 7a-g) and N-alkyl-3-(5-phenyl-1,3,4-oxadiazol-2-yl)-7- (trifluoromethyl) quinolin-4-amine derivatives (9a-f). Newly synthesized compounds were characterized by spectral studies. The structure of 9a was evidenced by X-ray crystallographic study. Synthesized compounds were screened for their antibacterial performance against Mycobacterium smegmatis and Pseudomonas aeruginosa. Antifungal activity was also carried out on the fungal stains Candida albicans and Penicillium chrysogenum. Compounds 7a and 9c showed significant antimicrobial activity against all the tested microorganisms. Among all the compounds, 6d and 6e showed the lowest MIC value of 6.25 μg mL -1 against Mycobacterium smegmatis indicating these compounds can be possible future antituberculosis agents. 2014 the Partner Organisations.

5-Substituted 2--7-trifluoromethyl-quinolin-3-yl>-1,3,4-oxadiazoles as Hypotensive Agents

Kumar, Ashok,Jaju, B. P.,Gurtu, S.,Sinha, J. N.,Shanker, K.

, p. 93 - 95 (2007/10/02)

The title compounds (IVa-h) have been synthesized starting from ethyl 7-trifluoromethyl-4-hydroxyquinoline-3-carboxylate and evaluated for their hypotensive activity.

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