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187585-44-0

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187585-44-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 187585-44-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,7,5,8 and 5 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 187585-44:
(8*1)+(7*8)+(6*7)+(5*5)+(4*8)+(3*5)+(2*4)+(1*4)=190
190 % 10 = 0
So 187585-44-0 is a valid CAS Registry Number.

187585-44-0SDS

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 2-(2-fluorophenyl)-3-nitrochromen-4-one

1.2 Other means of identification

Product number -
Other names 4h-1-benzopyran-4-one,2-(2-fluorophenyl)-3-nitro

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:187585-44-0 SDS

187585-44-0Downstream Products

187585-44-0Relevant articles and documents

Synthesis and in vitro cytotoxicity of a series of 3-aminoflavones

Dauzonne,Folleas,Martinez,Chabot

, p. 71 - 82 (2007/10/03)

To further understand the molecular requirements for the antiproliferative activity of flavonoids, a series of 3-aminoflavones and some of their derivatives were prepared and evaluated using L1210 murine leukemia. Our novel five-step synthetic approach required easily available substituted aromatic aldehydes as starting materials and proved more convenient and more general than previously reported methods. Our results in the 3-aminoflavones series indicated that the 4'-methoxy group is important for cytotoxic activity. Moreover, for the flavone-8-acetic analogs, a marked increase in potency was observed with the addition of a 3-amino or a 3-nitro group. Methoxy groups on the 6 and 7 positions of flavonoids (as in cirsiliol) also appear to be important for antiproliferative activity. These results are essential for the further understanding of the critical molecular requirements that lead to antiproliferative properties in the flavonoid series.

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