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S)-2-(((2'-(1H-tetrazol-5-yl)-[1,1'-biphenyl]-4-yl)Methyl)aMino)-3Methylbutanoic acid, a complex organic compound, is a specific ligand for the angiotensin II type 1 (AT1) receptor. It is characterized by its ability to modulate the renin-angiotensin-aldosterone system, a critical pathway in the regulation of blood pressure and fluid balance in the body.

676129-92-3

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676129-92-3 Usage

Uses

Used in Pharmaceutical Industry:
S)-2-(((2'-(1H-tetrazol-5-yl)-[1,1'-biphenyl]-4-yl)Methyl)aMino)-3Methylbutanoic acid is used as an antihypertensive agent for the treatment of high blood pressure. It functions by blocking the action of angiotensin II, a potent vasoconstrictor, thereby reducing blood pressure and alleviating the workload on the heart.
Used in Cardiology:
In the field of cardiology, S)-2-(((2'-(1H-tetrazol-5-yl)-[1,1'-biphenyl]-4-yl)Methyl)aMino)-3Methylbutanoic acid is utilized to manage congestive heart failure. Its ability to lower blood pressure and improve cardiac function makes it a valuable asset in the treatment of heart disease, enhancing patient outcomes and survival rates post-heart attack.
Despite its therapeutic benefits, S)-2-(((2'-(1H-tetrazol-5-yl)-[1,1'-biphenyl]-4-yl)Methyl)aMino)-3Methylbutanoic acid may also induce side effects such as dizziness, hypotension, and hyperkalemia, which underscores the importance of careful patient monitoring and dosage adjustment as needed.

Check Digit Verification of cas no

The CAS Registry Mumber 676129-92-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,6,1,2 and 9 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 676129-92:
(8*6)+(7*7)+(6*6)+(5*1)+(4*2)+(3*9)+(2*9)+(1*2)=193
193 % 10 = 3
So 676129-92-3 is a valid CAS Registry Number.

676129-92-3SDS

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 desvaleroyl valsartan

1.2 Other means of identification

Product number -
Other names (S)-3-methyl-2-((2'-(1H-tetrazol-5-yl)biphenyl-4-ylmethyl)amino)butyric acid

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:676129-92-3 SDS

676129-92-3Relevant academic research and scientific papers

Preparation method of valsartan nitrite remainder

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Paragraph 0019-0028, (2019/04/17)

The invention discloses a preparation method of valsartan nitrite remainder, which belongs to the technical field of a preparation method of a chemical drug midbody. Valsartan is used as a raw material to have hydrolysis and nitrosation reaction to prepar

An efficient and telescopic process for valsartan, an angiotensin II Receptor Blocker

Aalla, Sampath,Gilla, Goverdhan,Bojja, Yakambram,Anumula, Raghupathi Reddy,Vummenthala, Prabhakar Reddy,Padi, Pratap Reddy

scheme or table, p. 682 - 686 (2012/08/07)

An efficient, telescopic, and scalable process for an antihypertensive drug substance, valsartan with an overall yield of 58%, and ~99.9% purity is described. A simple, and safe process is developed for the recovery of tributyltin chloride from the tributyltin hydroxide, byproduct formed in the tetrazole ring construction, and reused in the synthesis of valsartan.

PROCESS FOR THE PREPARATION OF TETRAZOLE DERIVATIVES FROM ORGANO BORON AND ORGANO ALUMINIUM AZIDES

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Page/Page column 55, (2008/06/13)

The present invention relates to a method for preparing substituted tetrazoles, compounds obtained according to this method, new reactants and new tetrazole derivatives.

PROCESS FOR THE MANUFACTURE OF VALSARTAN

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Page 21-22, (2008/06/13)

The present invention relates to a process for the manufacture of Valsartan, an angiotensin receptor blocker (ARB; also called angiotension II receptor antagonist or AT1 receptor antagonist) and salts thereof, to novel intermediates and process steps.

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