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836608-01-6

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836608-01-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 836608-01-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,3,6,6,0 and 8 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 836608-01:
(8*8)+(7*3)+(6*6)+(5*6)+(4*0)+(3*8)+(2*0)+(1*1)=176
176 % 10 = 6
So 836608-01-6 is a valid CAS Registry Number.

836608-01-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,7-dimethoxy-2-(4-nitrophenyl)chromen-4-one

1.2 Other means of identification

Product number -
Other names 5,7-dimethoxy-4'-nitroflavone

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:836608-01-6 SDS

836608-01-6Relevant articles and documents

Collateral sensitivity of resistant MRP1-overexpressing cells to flavonoids and derivatives through GSH efflux

Lorendeau, Doriane,Dury, Lauriane,Genoux-Bastide, Estelle,Lecerf-Schmidt, Florine,Sim?es-Pires, Claudia,Carrupt, Pierre-Alain,Terreux, Rapha?l,Magnard, Sandrine,Di Pietro, Attilio,Boumendjel, Ahcène,Baubichon-Cortay, Hélène

, p. 235 - 245 (2014/07/21)

The multidrug resistance protein 1 (MRP1) is involved in multidrug resistance of cancer cells by mediating drug efflux out of cells, often in co-transport with glutathione (GSH). GSH efflux mediated by MRP1 can be stimulated by verapamil. In cells overexp

Efficient synthesis of nitroflavones by cyclodehydrogenation of 2prime;-hydroxychalcones and by the Baker-Venkataraman method

Barros, Ana I. R. N. A.,Silva, Artur M. S.

, p. 1505 - 1528 (2007/10/03)

Several nitroflavone derivatives were synthesized by cyclodehydrogenation of 2′-hydroxychalcones and by the Baker-Venkataraman approach, starting from 2′-hydroxyacetophenones and benzoic acid derivatives. Nitroflavones synthesised by the first synthetic a

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