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2-Selenophenecarbonyl chloride, 5-methyl- (8CI,9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

30468-07-6

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30468-07-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30468-07-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,4,6 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 30468-07:
(7*3)+(6*0)+(5*4)+(4*6)+(3*8)+(2*0)+(1*7)=96
96 % 10 = 6
So 30468-07-6 is a valid CAS Registry Number.

30468-07-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methylselenophene-2-carbonyl chloride

1.2 Other means of identification

Product number -
Other names 2-Selenophenecarbonylchloride,5-methyl

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:30468-07-6 SDS

30468-07-6Relevant academic research and scientific papers

Synthesis and in vitro anticancer activity of 6,7-methylenedioxy (or 5-hydroxy-6-methoxy)-2-(substituted selenophenyl)quinolin-4-one analogs

Chen, Chien-Ting,Hsu, Mei-Hua,Cheng, Yung-Yi,Liu, Chin-Yu,Chou, Li-Chen,Huang, Li-Jiau,Wu, Tian-Shung,Yang, Xiaoming,Lee, Kuo-Hsiung,Kuo, Sheng-Chu

experimental part, p. 6046 - 6056 (2012/02/05)

6,7-Methylenedioxy (or 5-hydroxy-6-methoxy)-2-(substituted selenophenyl)quinolin-4-ones and their isosteric compounds were synthesized and evaluated for anticancer activity. Structure-activity relationships (SAR) of these compounds were established. Among all tested compounds, 6,7-methylenedioxy-2-(5-methylselenophen-2-yl)quinolin-4-one (4d) was found to be the most promising anticancer agent. In screening against NCI's 60 human tumor cell line panel, 4d exhibited highly selective and potent inhibitory activity against MDA-MB-435 melanoma. Furthermore, the results of COMPARE analysis suggested that 4d is an antimitotic agent with a different mechanism of action from the conventional antimitotic agents, such as colchicine, vinca alkaloids and paclitaxel. Therefore, 4d was identified as a new lead compound that merits further optimization.

Synthesis of 1-benzyl-3-(5-hydroxymethyl-2-furyl)selenolo[3,2-c]pyrazole derivatives as new anticancer agents

Chou, Li-Chen,Huang, Li-Jiau,Hsu, Mei-Hua,Fang, Mei-Chi,Yang, Jai-Sing,Zhuang, Shi-Hong,Lin, Hui-Yi,Lee, Fang-Yu,Teng, Che-Ming,Kuo, Sheng-Chu

experimental part, p. 1395 - 1402 (2010/06/12)

As part of our continuing search for potential anticancer drug candidates among YC-1 analogs, 1, 3-disubstituted selenolo[3,2-c]pyrazole derivatives were synthesized and evaluated for their cytotoxicity against NCI-H226 non-small cell lung cancer and A-498 renal cancer cell lines. Significant cytotoxicity was observed in 3-(5-hydroxymethyl-2-furyl) derivatives (2, 33, 36 and 37). Among them, compound 2 was found to have the most potent activity. The mode of action of compound 2 seems to differ from those of the 175 anticancer agents listed in NCI's standard database and resembles that of YC-1. Thus, we recommend that compound 2 should be developed further as new drug candidate for treatment of non-small cell lung cancer and renal cancer.

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