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CAS

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Tetraethyl ranelate is a chemical compound that was used in the treatment of osteoporosis, known for its dual action of stimulating new bone formation while inhibiting the breakdown of existing bone. It is believed to possess anti-inflammatory properties, although concerns about potential cardiovascular risks have led to its withdrawal from the market in some countries and limited use in others. The ongoing research into its safety and effectiveness has resulted in its unavailability for prescription in several countries.

58194-26-6

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58194-26-6 Usage

Uses

Used in Pharmaceutical Industry:
Tetraethyl ranelate is used as a therapeutic agent for osteoporosis treatment, for its ability to increase bone formation and decrease bone resorption, thereby improving bone density and strength.
However, due to the concerns regarding its cardiovascular risks, its application in this industry has been significantly reduced or halted in various countries, pending further research and regulatory decisions.

Check Digit Verification of cas no

The CAS Registry Mumber 58194-26-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,1,9 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 58194-26:
(7*5)+(6*8)+(5*1)+(4*9)+(3*4)+(2*2)+(1*6)=146
146 % 10 = 6
So 58194-26-6 is a valid CAS Registry Number.
InChI:InChI=1/C20H26N2O8S/c1-5-27-15(23)9-13-14(10-21)19(31-18(13)20(26)30-8-4)22(11-16(24)28-6-2)12-17(25)29-7-3/h5-9,11-12H2,1-4H3

58194-26-6SDS

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 Diethyl 2,2'-((3-cyano-4-(2-ethoxy-2-oxoethyl)-5-(ethoxycarbonyl)thiophen-2-yl)azanediyl)diacetate

1.2 Other means of identification

Product number -
Other names ethyl 5-[bis(2-ethoxy-2-oxoethyl)amino]-4-cyano-3-(2-ethoxy-2-oxoethyl)thiophene-2-carboxylate

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:58194-26-6 SDS

58194-26-6Downstream Products

58194-26-6Relevant articles and documents

In a HPLC method for controlled for preparing high-purity of strontium ranelate method

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Paragraph 0044; 0047; 0050, (2017/07/14)

The invention discloses a method for preparing high-purity strontium ranelate through centralized control of the HPLC (High Performance Liquid Chromatography) method, and belongs to the field of pharmaceutical synthesis. The method comprises the following steps: (1) preparing a compound as shown in formula (II), namely, feeding a compound as shown in formula (I), tetrahydrofuran, anhydrous potassium carbonate and ethyl bromoacetate to a reaction kettle, and performing catalytic reaction through a catalyst, wherein the reaction endpoint is monitored through the HPLC; and (2) preparing a compound as shown in formula (III), namely, dropping a tetrahydrofuran solution in which the compound as shown in formula (II) is dissolved to inorganic aqueous alkali to saponify under the centralized control of the HPLC; performing reduced pressure distillation and filtering; regulating the pH (Power of Hydrogen) with hydrochloric acid; then adding a strontium chloride aqueous solution to obtain crude strontium ranelate which is characterized in that the purity is more than 99.7%, the single impurity is less than 0.1%, and the total impurity is less than 0.5%; and finally drying to obtain the targeted strontium ranelate. The strontium ranelate prepared by the method has the advantages that by means of the HPLC based centralized control, the optimal reaction time is determined and the refining and purifying steps are reduced; in addition, the method is simple in process, easy to control, high in product purity, less in waste liquid, low in energy consumption, relatively low in cost, and applicable to industrial production.

PROCESS FOR THE PREPARATION OF STRONTIUM RANELATE, INTERMEDIATE OR HYDRATES THEREOF

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Page/Page column 7, (2013/08/15)

The present invention relates to an improved process for the synthesis of strontium ranelate compound of formula I or its hydrates thereof. More particularly, the present invention relates to an economically viable and industrially feasible process for the preparation of strontium ranelate, intermediate or its hydrates thereof.

SUBSTANTIALLY PURE STRONTIUM RANELATE

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Page/Page column 19-20, (2011/10/31)

Provided herein is an improved, commercially viable and industrially advantageous process for the preparation of strontium ranelate, and its intermediates, in high yield and purity. Provided further herein is a highly pure strontium ranelate substantially free of impurities, and pharmaceutical compositions comprising highly pure strontium ranelate substantially free of impurities.

Synthesis of substituted thieno[2,3-b]pyrroles

Hongtao, Wei,Jin, Cai,Min, Sun,Min, Ji

, p. 236 - 238 (2008/02/07)

Thieno[2,3-b]pyrroles can be synthesized through three steps: Gewald synthesis, alkylation, and Thorpe-Ziegler cyclization. Diethyl 3,6-bis ((ethoxycarbonyl)methyl)-4-amino-6H-thieno-[2,3-b]pyrrole-2,5-dicarboxylate (13) has been obtained by one-pot method in DMF in good yield and high quality.

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