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2-Propyl-1H-imidazole-4,5-dicarboxylic acid dimethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

124750-59-0

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124750-59-0 Usage

Chemical Properties

White or off-white crystalline powder

Check Digit Verification of cas no

The CAS Registry Mumber 124750-59-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,7,5 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 124750-59:
(8*1)+(7*2)+(6*4)+(5*7)+(4*5)+(3*0)+(2*5)+(1*9)=120
120 % 10 = 0
So 124750-59-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H14N2O4/c1-4-5-6-11-7(9(13)15-2)8(12-6)10(14)16-3/h4-5H2,1-3H3,(H,11,12)

124750-59-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Propyl-1H-Imidazole-4,5-Dicarboxylic Acid Dimethyl Ester

1.2 Other means of identification

Product number -
Other names Dimethyl 2-propyl-1H-imidazole-4,5-dicarboxylate

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:124750-59-0 SDS

124750-59-0Relevant academic research and scientific papers

PROCESS FOR (5-METHYL-2-OXO-1,3-DIOXOLEN-4-YL)METHYL4-(1-HYDROXY-1-METHYLETHYL)-2-PROPYL-1-[4-[2-TETRAZOL-5-YL)PHENYL]PHENYL]METHYLIMIDAZOLE-5-CARBOXYLATE

-

Page/Page column 18, (2011/04/13)

The present invention relates to an improved process for the preparation of (5-methyl-2-oxo- 1,3-dioxolen-4-yl)methyl4-(1-hydroxy- 1-methylethyl)-2-propyl-1-[4-[2-(tetrazol-5-yl)phenyl]phenyl]methyl imidazole-5-carboxylate.

Efficient synthesis of olmesartan medoxomil, an antihypertensive drug

Babu, Karrothu Srihari,Reddy, Mallepalli Srinivasa,Tagore, Amirisetty Ravindranath,Reddy, Gade Srinivas,Sebastian, Sony,Varma, Mudunuru Satish,Venkateswarlu, Gandu,Bhattacharya, Apurba,Reddy, Padi Pratap,Anand, Ramasamy Vijaya

experimental part, p. 291 - 298 (2009/05/07)

This document describes a simple and robust process for the synthesis of olmesartan medoxomil. This tailored process allows us to synthesize olmesartan medoxomil on a large scale with 50% overall yield. Also, our process has excellent control of the impurity profile in all the stages. Copyright Taylor & Francis Group, LLC.

PROCESS FOR PREPARING OLMESARTAN MEDOXOMIL

-

Page/Page column 19-20, (2008/06/13)

A process for preparing olmesartan medoxomil.

Fused aryl substituted imidazole angiotensin II receptor inhibitors

-

, (2008/06/13)

Substituted imidazoles such as STR1 which are useful as angiotensin II receptor inhibitors. These compounds have activity in treating hypertension and congestive heart failure.

ANGIOTENSIN II RECEPTOR BLOCKING IMIDAZOLES

-

, (2008/06/13)

Substituted imidazoles such as STR1 are useful as angiotensin II blockers. These compounds have activity in treating hypertension and congestive heart failure.

Treatment of congestive heart failure with angiotensin 11 receptor blocking imidazoles

-

, (2008/06/13)

Substituted imidazoles such as STR1 are useful as angiotensin II blockers. These compounds have activity in treating hypertension and congestive heart failure.

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