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59987-31-4

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59987-31-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59987-31-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,9,8 and 7 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 59987-31:
(7*5)+(6*9)+(5*9)+(4*8)+(3*7)+(2*3)+(1*1)=194
194 % 10 = 4
So 59987-31-4 is a valid CAS Registry Number.

59987-31-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (7-nitro-2,3-dihydrobenzo[b][1,4]dioxin-2-yl)methanol

1.2 Other means of identification

Product number -
Other names (7-nitro-2,3-dihydro-benzo[1,4]dioxin-2-yl)-methanol

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:59987-31-4 SDS

59987-31-4Relevant articles and documents

3-(Benzodioxan-2-ylmethoxy)-2,6-difluorobenzamides bearing hydrophobic substituents at the 7-position of the benzodioxane nucleus potently inhibit methicillin-resistant Sa and Mtb cell division

Straniero, Valentina,Pallavicini, Marco,Chiodini, Giuseppe,Zanotto, Carlo,Volontè, Luca,Radaelli, Antonia,Bolchi, Cristiano,Fumagalli, Laura,Sanguinetti, Maurizio,Menchinelli, Giulia,Delogu, Giovanni,Battah, Basem,De Giuli Morghen, Carlo,Valoti, Ermanno

, p. 227 - 243 (2016/05/24)

Lipophilic substituents at benzodioxane C (7) of 3-(benzodioxan-2-ylmethoxy)-2,6-difluorobenzamide improve the antibacterial activity against methicillin-resistant Staphylococcus aureus strains to MIC values in the range of 0.2-2.5 μg/mL, whereas hydrophi

OXINDOLEDIOXANS, SYNTHESIS THEREOF, AND INTERMEDIATES THERETO

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Page/Page column 12, (2008/06/13)

The present invention provides methods for preparing compounds having activity as dopamine autoreceptor agonists and partial agonists at the postsynaptic dopamine D2 receptor. These compounds are useful for treating dopaminergic disorders, such

Amide derivatives as ion-channel ligands and pharmaceutical compositions and methods of using the same

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Page/Page column 31, (2010/11/23)

Compounds are disclosed that have a formula represented by the following: The compounds may be prepared as pharmaceutical compositions, and may be used for the prevention and treatment of a variety of conditions in mammals including humans, including by way of non-limiting example, pain, inflammation, traumatic injury, and others.

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