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Ethanol, 2-[[(4-nitrophenyl)methyl]thio]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

98288-50-7

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98288-50-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98288-50-7 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, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 98288-50:
(7*9)+(6*8)+(5*2)+(4*8)+(3*8)+(2*5)+(1*0)=187
187 % 10 = 7
So 98288-50-7 is a valid CAS Registry Number.

98288-50-7SDS

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-(4-nitrobenzylthio)ethanol

1.2 Other means of identification

Product number -
Other names 2-(4-nitro-benzylsulfanyl)-ethanol

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:98288-50-7 SDS

98288-50-7Relevant academic research and scientific papers

ANTHRANILAMIDE INHIBITORS OF AURORA KINASE

-

Page/Page column 39, (2008/12/07)

The present invention relates to a compound represented by the following formula: or a pharmaceutically acceptable salt thereof; where R1, R2, R3, R4, r and s are as previously defined. Compounds of the present invention are useful in the treatment of diseases associated with Aurora kinase activity such as cancer.

Ar(alk)ylsulfonyl ethyl groups as phosphorus-protecting functions

Claesen, C. A. A.,Segers, R. P. A. M.,Tesser, G. I.

, p. 119 - 122 (2007/10/02)

Various 2-ethanols were prepared and subsequently converted into the corresponding phosphorodichloridites in almost quantitative yield via a convenient synthetic route.The versatility of the method, which obviates the necessity of a distillation step, is demonstrated by the preparation of other (Ar(alk)yl phosphorodichloridites, including the unstable benzyl phosphorodichloridite.

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