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133999-06-1

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133999-06-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133999-06-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,9,9 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 133999-06:
(8*1)+(7*3)+(6*3)+(5*9)+(4*9)+(3*9)+(2*0)+(1*6)=161
161 % 10 = 1
So 133999-06-1 is a valid CAS Registry Number.

133999-06-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-chloro-4,4-dimethyl-1,3-dihydroquinolin-2-one

1.2 Other means of identification

Product number -
Other names 2(1H)-Quinolinone,7-chloro-3,4-dihydro-4,4-dimethyl

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:133999-06-1 SDS

133999-06-1Downstream Products

133999-06-1Relevant articles and documents

Synthesis and anticancer activity of aminodihydroquinoline analogs: Identification of novel proapoptotic agents

Lee, Eun,Han, Seulaa,Jin, Guo Hua,Lee, Hwa Jin,Kim, Woo-Young,Ryu, Jae-Ha,Jeon, Raok

supporting information, p. 3976 - 3978 (2013/07/25)

A series of 2-aminodihydroquinoline analogs were synthesized and their in vitro cytotoxicities against metastatic breast adenocarcinoma cell line MDA-MB-231 were tested. Five out of 16 compounds exhibited promising activity and structure-activity relationship revealed major role of dialkylaminoethyl substituents on dihydroquinoline ring for the activity. Two compounds, 5f and 5h, presented cytotoxicity with IC50 values of about 2 μM when the compounds were treated to the cells without serum. The cell proliferation was inhibited mildly when the cells cultured with serum. Flow cytometry analyses showed that those compounds arrested the cells at G2/M checkpoint when the cell cycle is active while they induce apoptosis when the cell growth is restricted due to the absence of growth factors. These results suggest the two novel compounds may have anticancer activity through cell cycle arrest and pro apoptosis mechanism.

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