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2-Propen-1-one, 1-(2-hydroxy-1-naphthalenyl)-3-(4-methylphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38280-30-7

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38280-30-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38280-30-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,2,8 and 0 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 38280-30:
(7*3)+(6*8)+(5*2)+(4*8)+(3*0)+(2*3)+(1*0)=117
117 % 10 = 7
So 38280-30-7 is a valid CAS Registry Number.

38280-30-7SDS

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 1-(2-hydroxynaphthalen-1-yl)-3-(4-methylphenyl)prop-2-en-1-one

1.2 Other means of identification

Product number -
Other names 2-Propen-1-one,1-(2-hydroxy-1-naphthalenyl)-3-(4-methylphenyl)

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:38280-30-7 SDS

38280-30-7Relevant academic research and scientific papers

Fungal metabolism of naphthoflavones

Pop?oński, Jaros?aw,Sordon, Sandra,Tronina, Tomasz,Bartmańska, Agnieszka,Huszcza, Ewa

, p. 1 - 6 (2015/05/05)

Naphthoflavones (benzoflavones) are synthetic flavonoids commonly used in drug metabolism studies as selective activators or inhibitors of cytochrome P-450 enzymes. Nowadays they are also used as a component of food supplements for body builders. There is

Ruthenium(II) chalconate complexes: Synthesis, characterization, catalytic, and biological studies

Muthukumar,Viswanathamurthi

experimental part, p. 454 - 462 (2009/10/30)

A series of new hexa-coordinated ruthenium(II) carbonyl complexes of the type [RuCl(CO)(EPh3)(B)(L)] (E = P or As; B = PPh3, AsPh3 or Py; L = 2′-hydroxychalcones) have been prepared by reacting [RuHCl(CO)(EPh3)2(B)] (E = P or As; B = PPh3, AsPh3 or Py) with 2′-hydroxychalcones in benzene under reflux. The new complexes have been characterized by analytical and spectral (IR, electronic, 1H, 31P and 13C NMR) data. Based on the above data, an octahedral structure has been assigned for all the complexes. The new complexes exhibit catalytic activity for the oxidation of primary and secondary alcohols into their corresponding aldehydes and ketones in the presence of N-methylmorpholine-N-oxide (NMO) as co-oxidant and also found efficient catalyst in the transfer hydrogenation of ketones. The antifungal properties of the complexes have also been examined and compared with standard Bavistin.

Condensed 1,8-Naphthyridines. Part-VI. Synthesis of 8-Aryl-8H-naphthopyranonaphthyridines

Reddy, K. Rajendar,Mogilaiah, K.,Sreenivasulu, B.

, p. 984 - 985 (2007/10/02)

The condensation of 2-aminonicotinaldehyde (1) with substituted-2-hydroxy-1-naphthyl styryl ketones (2) in the presence of glacial acetic acid containing a catalytic amount of concentrated sulphuric acid affords the corresponding 8-aryl-8H-naphtho1',2':5

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