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195385-87-6

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195385-87-6 Usage

General Description

1(2H)-Naphthalenone, 3,4-dihydro-5-(β-D-ribofuranosyloxy)- is a chemical compound with the molecular formula C15H18O6. It is a derivative of naphthalenone and is a naturally occurring organic compound found in certain plant species such as Damson plums. This chemical is known for its potential pharmacological and biological activities, including anti-inflammatory properties. It has also been studied for its potential antioxidant and anti-cancer properties. The compound is a ribofuranoside derivative and can be synthesized for research and medical purposes.

Check Digit Verification of cas no

The CAS Registry Mumber 195385-87-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,5,3,8 and 5 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 195385-87:
(8*1)+(7*9)+(6*5)+(5*3)+(4*8)+(3*5)+(2*8)+(1*7)=186
186 % 10 = 6
So 195385-87-6 is a valid CAS Registry Number.

195385-87-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-tetralone-5-yl β-D-ribofuranoside

1.2 Other means of identification

Product number -
Other names -

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:195385-87-6 SDS

195385-87-6Upstream product

195385-87-6Downstream Products

195385-87-6Relevant articles and documents

ENZYME DETECTION/ASSAY METHOD AND SUBSTRATES

-

, (2008/06/13)

The invention relates to a method of detecting and/or assaying nucleoside hydrolases or nucleoside phosphorylases using a chromogenic substrate. Preferred chromogenic substrates have formula (I) where X is OH, or H, and Y is the residue of Y—OH where Y—OH is a chromophore or a compound readily converted to a chromophore and the substrates are hydrolysed by the nucleoside hydrolase to yield ribose or 2-deoxyribose plus Y—OH. Alternatively those substrates may be phosphorylysed by nucleoside phosphorylase to yield ribose-1-phosphate plus Y—OH. The methods may be used to detect and/or assay parasites in biological samples.

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