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The chemical with the CAS number 90389-12-1 is known as 1-(4-Methylphenyl)-3-phenylprop-2-en-1-one, which is a derivative of chalcone. 90389-12-1 is characterized by a phenyl group attached to a chalcone structure, featuring a carbonyl group and an alpha, beta-unsaturated ketone system. It is often used in the synthesis of various pharmaceuticals and organic compounds due to its reactive nature and the potential for further functionalization. The compound is typically handled in a laboratory setting due to its chemical reactivity and should be used with appropriate safety measures.

90390-17-3

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90390-17-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90390-17-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,3,9 and 0 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 90390-17:
(7*9)+(6*0)+(5*3)+(4*9)+(3*0)+(2*1)+(1*7)=123
123 % 10 = 3
So 90390-17-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H11Cl2N/c1-2-12-6-7-5-8(10)3-4-9(7)11/h3-5,12H,2,6H2,1H3

90390-17-3SDS

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 (2,5-Dichloro-benzyl)-ethyl-amine

1.2 Other means of identification

Product number -
Other names (2,5-Dichloro-benzyl)-ethyl-amine

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:90390-17-3 SDS

90390-17-3Upstream product

90390-17-3Downstream Products

90390-17-3Relevant academic research and scientific papers

Benzylamines: Synthesis and evaluation of antimycobacterial properties

Meindl,Von Angerer,Schonenberger,Ruckdeschel

, p. 1111 - 1118 (2007/10/02)

The synthesis of benzylamines with various N-alkyl chains and substituents in the aromatic system as well as their evaluation on Mycobacterium tuberculosis H 37 Ra are described. The most active compounds in this test, N-methyl-3-chlorobenzylamine (MIC 10.2 μg/mL), N-methyl-3,5-dichlorobenzylamine (93, MIC 10.2 μg/mL), and N-butyl-3,5-difluorobenzylamine (MIC 6.4 μg/mL), also exhibited a marked inhibitory effect on Mycobacterium marinum and Mycobacterium lufu used for the determination of antileprotic properties. The combination of 93 with aminosalicylic acid, streptomycin, or dapsone exert marked supra-additive effects on M. tuberculosis H 37 Ra.

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