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spiro[adamantane-2,4'-imidazolidine]-2',5'-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

50346-47-9

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50346-47-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50346-47-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,3,4 and 6 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 50346-47:
(7*5)+(6*0)+(5*3)+(4*4)+(3*6)+(2*4)+(1*7)=99
99 % 10 = 9
So 50346-47-9 is a valid CAS Registry Number.

50346-47-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(2-hydroxyethyl)-5-methyl-2-methylsulfanyl-1H-[1,2,4]triazolo[1,5-a]pyrimidin-7-one,3-methylsulfanyl-1H-1,2,4-triazol-5-amine

1.2 Other means of identification

Product number -
Other names 9-Phenanthrenebutanoic 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:50346-47-9 SDS

50346-47-9Relevant academic research and scientific papers

The synthesis of neurotensin antagonist SR 48692 for prostate cancer research

Baxendale,Cheung,Kitching,Ley,Shearman

, p. 4378 - 4387 (2013/07/27)

An improved synthesis of the molecule SR 48692 is presented and its use as a neurotensin antagonist biological probe for use in cancer research is described. The preparation includes an number of enhanced chemical conversions and strategies to overcome some of the limiting synthetic transformations in the original chemical route.

A flow-based synthesis of 2-aminoadamantane-2-carboxylic acid

Battilocchio, Claudio,Baxendale, Ian R.,Biava, Mariangela,Kitching, Matthew O.,Ley, Steven V.

supporting information; experimental part, p. 798 - 810 (2012/08/27)

The development of a new, high-yielding, scalable and safe process for the preparation of 2-aminoadamantane-2-carboxylic acid (1) is described. This geminal, functionalized achiral amino acid has been reported to possess interesting biological activity as

N-[2-(nitro-1-imidazolyl)ethyl]naphthal imides

-

, (2008/06/13)

Imides having a nitroimidazolylethyl group as a N-substituent are described herein. They are anti-bacterial and anti-protozoal agents. The compounds are prepared by the reaction of the appropriate imide with the chloroethylimidazole or with the tosylate or mesylate of the corresponding hydroxyethyl compound.

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