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1H-Isoindole-5-carboxylic acid, 2-[2,6-bis(1-methylethyl)phenyl]-2,3-dihydro-1,3-dioxo- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

100844-12-0

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100844-12-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100844-12-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,8,4 and 4 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 100844-12:
(8*1)+(7*0)+(6*0)+(5*8)+(4*4)+(3*4)+(2*1)+(1*2)=80
80 % 10 = 0
So 100844-12-0 is a valid CAS Registry Number.

100844-12-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-carboxy-2-(2,6-diisopropylphenyl)-1H-isoindole-1,3-dione

1.2 Other means of identification

Product number -
Other names TCA-33

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:100844-12-0 SDS

100844-12-0Relevant academic research and scientific papers

Development of tubulin-polymerization inhibitors based on the thalidomide skeleton

Aoyama, Hiroshi,Noguchi, Tomomi,Misawa, Takashi,Nakamura, Takanori,Miyachi, Hiroyuki,Hashimoto, Yuichi,Kobayashi, Hisayoshi

, p. 944 - 949 (2008/02/09)

We synthesized a series of compounds based on the potent tubulin-polymerization inhibitor 5-hydroxy-2-(2,6-diisopropylphenyl)-1H- isoindole-1,3-dione [5HPP-33 (3)], which is structurally derived from thalidomide (1), and investigated their inhibitory effe

Inhibitors of NF-κB derived from thalidomide

Carcache de-Blanco, Esperanza J.,Pandit, Bulbul,Hu, Zhigen,Shi, Jiandong,Lewis, Andrew,Li, Pui-Kai

, p. 6031 - 6035 (2008/09/17)

A series of compounds originally derived from thalidomide were synthesized and evaluated. The most potent compounds in this series, 5HPP-33 and compound 20, inhibited NF-κB activation in HeLa cells. Preliminary study indicated that the mechanism of inhibition of NF-κB activation is through inhibition of its translocation from the cytoplasm to the nucleus.

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