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2,4-Pyrimidinediamine, 5-((3,4,5-trimethoxyphenyl)methyl)-, monohydrat e is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69449-07-6

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69449-07-6 Usage

Structure

Pyrimidine ring with two amino groups and a 5-((3,4,5-trimethoxyphenyl)methyl) group

Uses

Synthesis of pharmaceuticals, potential applications in medicinal chemistry

Properties

Biological or pharmacological properties of interest in research and development

Hydrate form

Monohydrate, indicating one water molecule per chemical molecule

Industrial and scientific applications

Potential for use in the synthesis of pharmaceuticals and other industrial and scientific applications.

Check Digit Verification of cas no

The CAS Registry Mumber 69449-07-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,4,4 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 69449-07:
(7*6)+(6*9)+(5*4)+(4*4)+(3*9)+(2*0)+(1*7)=166
166 % 10 = 6
So 69449-07-6 is a valid CAS Registry Number.
InChI:InChI=1/C14H18N4O3.H2O/c1-19-10-5-8(6-11(20-2)12(10)21-3)4-9-7-17-14(16)18-13(9)15;/h5-7H,4H2,1-3H3,(H4,15,16,17,18);1H2

69449-07-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-[(3,4,5-trimethoxyphenyl)methyl]pyrimidine-2,4-diamine,hydrate

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:69449-07-6 SDS

69449-07-6Downstream Products

69449-07-6Relevant academic research and scientific papers

Tetramorphs of the antibiotic drug trimethoprim: Characterization and stability

Maddileti,Swapna, Battini,Nangia, Ashwini

, p. 1745 - 1756 (2015/04/14)

Trimethoprim (TMP) is a well-known antifolate drug and one of the most widely used broad-spectrum antibiotics. TMP was first approved by the United States FDA in combination with sulfamethoxazole (SMZ) in 1973, and three polymorphs of TMP (named Form I, II, and III) and a hydrate form were reported in 1978. However, a complete characterization and molecular level analysis of polymorphic structures are not available. We report herein four polymorphs (Forms 1-4) of TMP and a hemihydrate form with complete structural and thermal characterization. The polymorphs were isolated in the pure state by different techniques such as antisolvent method, freeze-drying, and spray drying. Polymorphs 1 and 2 of our study match with Forms I and II reported, and polymorphs 3 and 4 are novel. The X-ray crystal structure of a novel TMP Form 2 is now reported nearly four decades after the first crystal structure of Form 1 was determined by neutron diffraction (J. Am. Chem. Soc. 1976, 98, 2074-2078). The crystal structure of Form 1 has two types of R22(8) motifs, and Form 2 has a third type R22(8) and R32(8) motif of N-H...Narom hydrogen bonds. The polymorphs were characterized by FT-IR and Raman spectroscopy, differential scanning calorimetry (DSC), 15N ss-NMR, field emission scanning electron microscopy, powder X-ray diffraction, and also dynamic vapor sorption. Thermodynamic stability, phase transformations, and Hirshfeld surfaces are also discussed. The polymorphs were tested under accelerated International Conference on Harmonization (ICH) conditions of 40 C and 75% RH for stability, and found that all the solid forms were stable for three months except TMP Form 3, which converted to Form 2. Slurry grinding and thermal experiments suggest that TMP Form 1 is the most stable modification among TMP crystal forms.

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