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Acetic acid, [[(3-bromophenyl)methyl]thio]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

98288-01-8

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98288-01-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98288-01-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,2,8 and 8 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 98288-01:
(7*9)+(6*8)+(5*2)+(4*8)+(3*8)+(2*0)+(1*1)=178
178 % 10 = 8
So 98288-01-8 is a valid CAS Registry Number.

98288-01-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(3-bromophenyl)methylsulfanyl]acetic acid

1.2 Other means of identification

Product number -
Other names [(3-bromobenzyl)thio]acetic acid

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:98288-01-8 SDS

98288-01-8Relevant academic research and scientific papers

Design, synthesis and preliminary biological evaluation of benzylsulfone coumarin derivatives as anti-cancer agents

Wang, Tao,Peng, Tao,We, Xiaoxue,Wang, Gang,Sun, Yunbo,Liu, Shuchen,Zhang, Shouguo,Wang, Lin

, (2019)

In this work, a series of benzylsulfone coumarin derivatives 5a-5o were synthesized and characterized. Kinase inhibitory activity assay indicated that most of the compounds showed considerable activity against PI3K. Anti-tumor activity studies of the active compounds were also carried out in vitro on the Hela, HepG2, H1299, HCT-116, and MCF-7 tumor cell lines by MTS assay. The structure-activity relationships (SARs) of these compounds were analyzed in detail. Compound 5h exhibited the most potent activities against the mentioned cell lines with IC50 values ranging from 18.12 to 32.60 μM, followed by 5m with IC50 values of 29.30-42.14 μM. Furthermore, 5h and 5m clearly retarded the migration of Hela cells in vitro. Next, an in silico molecular docking study was conducted to evaluate the binding models of 5h and 5m towards PI3Kαand PI3Kβ. Collectively, the above findings suggested that compounds 5h and 5m might be promising PI3K inhibitors deserving further investigation for cancer treatment.

EFFECT OF MOLECULAR STRUCTURE ON OPTICAL PROPERTIES OF SULFOXIDE SYSTEMS. m-BROMOBENZYLSULFINYLACETIC ACIDS AND SOME OF THEIR DERIVATIVES. PART VII

Janczewski, Marian,Ksiezopolski, Jerzy

, p. 103 - 116 (2007/10/02)

The synthesis and principal properties of m-bromobenzylsulfinylacetic and m-bromobenzylsulfonylacetic acids are described.Racemic sulfoxide was resolved by crystallization of its diastereomeric salts with optically active bases.The absolute configuration

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