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6-fluoro-2-methyl-3-vinylbenzonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1255207-48-7

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1255207-48-7 Usage

Derivative of

Benzonitrile

Functional Groups

Fluorine atom (6th position), Methyl group (2nd position), Vinyl group (3rd position)

Common Uses

Production of pharmaceuticals and agrochemicals, synthesis of organic compounds

Applications

Medicinal chemistry, building block for new drugs and biologically active molecules

Safety Concerns

Handle with caution to prevent potential hazards to human health and the environment

Check Digit Verification of cas no

The CAS Registry Mumber 1255207-48-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,5,2,0 and 7 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1255207-48:
(9*1)+(8*2)+(7*5)+(6*5)+(5*2)+(4*0)+(3*7)+(2*4)+(1*8)=137
137 % 10 = 7
So 1255207-48-7 is a valid CAS Registry Number.

1255207-48-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-ethenyl-6-fluoro-2-methylbenzonitrile

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:1255207-48-7 SDS

1255207-48-7Downstream Products

1255207-48-7Relevant academic research and scientific papers

INHIBITORS OF THE RENAL OUTER MEDULLARY POTASSIUM CHANNEL

-

, (2016/10/06)

The present invention provides compounds of Formula Ia and the pharmaceutically acceptable salts thereof, which are inhibitors of the ROMK (Kir1.1) channel. The compounds may be used as diuretic and/or natriuretic agents and for the therapy and prophylaxis of medical conditions including cardiovascular diseases such as hypertension, heart failure and conditions associated with excessive salt and water retention.

Discovery of a potent and selective ROMK inhibitor with improved pharmacokinetic properties based on an octahydropyrazino[2,1-c][1,4]oxazine scaffold

Zhu, Yuping,de Jesus, Reynalda K.,Tang, Haifeng,Walsh, Shawn P.,Jiang, Jinlong,Gu, Xin,Teumelsan, Nardos,Shahripour, Aurash,Pio, Barbara,Ding, Fa-Xiang,Ha, Sookhee,Priest, Birgit T.,Swensen, Andrew M.,Alonso-Galicia, Magdalena,Felix, John P.,Brochu, Richard M.,Bailey, Timothy,Thomas-Fowlkes, Brande,Zhou, Xiaoyan,Pai, Lee-Yuh,Hampton, Caryn,Hernandez, Melba,Owens, Karen,Ehrhart, Juliann,Roy, Sophie,Kaczorowski, Gregory J.,Yang, Lihu,Parmee, Emma R.,Sullivan, Kathleen,Garcia, Maria L.,Pasternak, Alexander

, p. 5695 - 5702 (2016/11/29)

Following the discovery of small molecule acyl piperazine ROMK inhibitors, the acyl octahydropyrazino[2,1-c][1,4]oxazine series was identified. This series displays improved ROMK/hERG selectivity, and as a consequence, the resulting ROMK inhibitors do not evoke QTc prolongation in an in vivo cardiovascular dog model. Further efforts in this series led to the discovery of analogs with improved pharmacokinetic profiles. This new series also retained comparable ROMK potency compared to earlier leads.

INHIBITORS OF THE RENAL OUTER MEDULLARY POTASSIUM CHANNEL

-

, (2014/07/08)

The present invention provides compounds of Formula I and the pharmaceutically acceptable salts thereof, which are inhibitors of the ROMK (Kirl.1) channel. The compounds may be used as diuretic and/or natriuretic agents and for the therapy and prophylaxis of medical conditions including cardiovascular diseases such as hypertension, heart failure and conditions associated with excessive salt and water retention.

INHIBITORS OF THE RENAL OUTER MEDULLARY POTASSIUM CHANNEL

-

, (2014/09/03)

The present invention provides compounds of Formula(I) or a pharmaceutically acceptable salt thereof, which are inhibitors of the ROMK (Kir1.1) channel. The compounds may be used as diuretic and/or natriuretic agents and for the therapy and prophylaxis of medical conditions including cardiovascular diseases such as hypertension, heart failure, kidney disease, edema, and conditions associated with excessive salt and water retention.

INHIBITORS OF THE RENAL OUTER MEDULLARY POTASSIUM CHANNEL

-

, (2014/06/23)

The present invention provides compounds of Formula (I), and the pharmaceutically acceptable salts thereof, which are inhibitors of the ROMK (Kir1.1) channel. The compounds may be used as diuretic and/or natriuretic agents and for the therapy and prophyla

INHIBITORS OF THE RENAL OUTER MEDULLARY POTASSIUM CHANNEL

-

, (2013/07/05)

The present invention provides compounds of Formula (I) and the pharmaceutically acceptable salts thereof, which are inhibitors of the ROMK (Kir1.1) channel. The compounds act as diuretics and natriuretics and are valuable pharmaceutically active compounds for the therapy and prophylaxis of medical conditions including cardiovascular diseases such as hypertension and conditions resulting from excessive salt and water retention.

INHIBITORS OF THE RENAL OUTER MEDULLARY POTASSIUM CHANNEL

-

, (2013/03/26)

The present invention provides compounds of Formula Ia and the pharmaceutically acceptable salts thereof, which are inhibitors of the ROMK (Kir1.1) channel. The compounds may be used as diuretic and/or natriuretic agents and for the therapy and prophylaxis of medical conditions including cardiovascular diseases such as hypertension, heart failure and conditions associated with excessive salt and water retention.

INHIBITORS OF THE RENAL OUTER MEDULLARY POTASSIUM CHANNEL

-

Page/Page column 67, (2010/11/18)

This invention relates to compounds having structural Formula I: and pharmaceutically acceptable salts thereof which are inhibitors of the Renal Outer Medullary Potassium (ROMK) channel (Kir1.1). The compounds of Formula I are useful as diuretics and natriuretics and therefore are useful for the therapy and prophylaxis of disorders resulting from excessive salt and water retention, including cardiovascular diseases such as hypertension and chronic and acute heart failure

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