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2-hydroxybenzoic acid - pyridine-3-carboxamide (1:1) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

66634-12-6

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66634-12-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66634-12-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,6,3 and 4 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 66634-12:
(7*6)+(6*6)+(5*6)+(4*3)+(3*4)+(2*1)+(1*2)=136
136 % 10 = 6
So 66634-12-6 is a valid CAS Registry Number.

66634-12-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hydroxybenzoic acid,pyridine-3-carboxamide

1.2 Other means of identification

Product number -
Other names Nicotinamide salicylate

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:66634-12-6 SDS

66634-12-6Downstream Products

66634-12-6Relevant academic research and scientific papers

Experimental and Theoretical Study of Selectivity in Mechanochemical Cocrystallization of Nicotinamide with Anthranilic and Salicylic Acid

Lukin, Stipe,Lon?ari?, Ivor,Tireli, Martina,Stolar, Tomislav,Blanco, Maria V.,Lazi?, Predrag,U?arevi?, Krunoslav,Halasz, Ivan

, p. 1539 - 1547 (2018)

Selectivity in mechanochemical cocrystal formation between nicotinamide and anthranilic acid or salicylic acid was studied using tandem in situ reaction monitoring by powder X-ray diffraction (PXRD) and Raman spectroscopy. Selectivity was probed by offering a competing cocrystal coformer to a previously prepared cocrystal or under competitive reaction conditions where all cocrystal coformers, in different stoichiometric ratios, were introduced together in the starting reaction mixture. Reaction paths were dependent on the starting mixture composition, and we find that the formation of intermediates and the final product can be predicted from solid-state ab initio calculations of relative energies of possible reaction mixtures. In some cases, quantitative assessment revealed different reaction profiles derived from PXRD and Raman monitoring, directly indicating, for the first time, different mechanochemical reactivity on the molecular and the bulk crystalline level of the reaction mixture.

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