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Ethyl 5-Amino-1-(2-fluorobenzyl)-1H-pyrazole-3-carboxylate is an organic compound with a complex chemical structure. It is characterized by its potential applications in various fields, particularly as a stimulator of soluble guanylate cyclase.

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  • 256504-39-9 Structure
  • Basic information

    1. Product Name: ethyl 5-aMino-1-(2-fluorobenzyl)-1H-pyrazole-3-carboxylate
    2. Synonyms: ethyl 5-aMino-1-(2-fluorobenzyl)-1H-pyrazole-3-carboxylate;5-Amino-1-[(2-fluorophenyl)methyl]-1H-pyrazole-3-carboxylic acid ethyl ester
    3. CAS NO:256504-39-9
    4. Molecular Formula: C13H14FN3O2
    5. Molecular Weight: 263.2675632
    6. EINECS: -0
    7. Product Categories: Riociguat
    8. Mol File: 256504-39-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 451.9±40.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.29±0.1 g/cm3(Predicted)
    6. Vapor Pressure: 0Pa at 20℃
    7. Refractive Index: N/A
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 1.50±0.10(Predicted)
    11. CAS DataBase Reference: ethyl 5-aMino-1-(2-fluorobenzyl)-1H-pyrazole-3-carboxylate(CAS DataBase Reference)
    12. NIST Chemistry Reference: ethyl 5-aMino-1-(2-fluorobenzyl)-1H-pyrazole-3-carboxylate(256504-39-9)
    13. EPA Substance Registry System: ethyl 5-aMino-1-(2-fluorobenzyl)-1H-pyrazole-3-carboxylate(256504-39-9)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 256504-39-9(Hazardous Substances Data)

256504-39-9 Usage

Uses

Used in Pharmaceutical Research:
Ethyl 5-Amino-1-(2-fluorobenzyl)-1H-pyrazole-3-carboxylate is used as a research compound for the development of new drugs targeting soluble guanylate cyclase. This enzyme plays a crucial role in the regulation of vascular tone and blood flow, making it a potential therapeutic target for conditions such as hypertension, heart failure, and pulmonary hypertension.
Used in Soluble Guanylate Cyclase Stimulation Studies:
In the field of biomedical research, ethyl 5-Amino-1-(2-fluorobenzyl)-1H-pyrazole-3-carboxylate is used as a stimulator of soluble guanylate cyclase for investigating its potential effects on cellular signaling pathways and physiological responses. This application aids in understanding the underlying mechanisms of various diseases and the development of novel therapeutic strategies.
Used in Drug Development for Cardiovascular Diseases:
Ethyl 5-Amino-1-(2-fluorobenzyl)-1H-pyrazole-3-carboxylate is utilized as a key compound in the development of drugs aimed at treating cardiovascular diseases. By stimulating soluble guanylate cyclase, it may help in the regulation of blood vessel dilation and overall cardiovascular function, offering potential benefits for patients suffering from conditions such as hypertension and heart failure.

Check Digit Verification of cas no

The CAS Registry Mumber 256504-39-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,6,5,0 and 4 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 256504-39:
(8*2)+(7*5)+(6*6)+(5*5)+(4*0)+(3*4)+(2*3)+(1*9)=139
139 % 10 = 9
So 256504-39-9 is a valid CAS Registry Number.

256504-39-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 5-amino-1-(2-fluorobenzyl)-1H-pyrazole-3-carboxylate

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:256504-39-9 SDS

256504-39-9Downstream Products

256504-39-9Relevant articles and documents

PROCESS FOR THE PREPARATION OF METHYL 4,6-DIAMINO-2-[L-(2-FHIOROBENZVR)-LH-PYRAZOLO I3,4-BLPVRIDIN-3-VN-5-PYRIMIDINYL(METHVL)CARBAMATE AND ITS POLYMORPHS THEREOF

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Page/Page column 31; 32, (2017/03/08)

The present invention relates to process for the preparation of methyl 4,6-diamino-2-[1-(2-fluorobenzyl)-lH-pyrazolo[3,4-b]pyridin-3-yl]-5-pyrimidinyl(methyl)carbamate and its polymorphs thereof compound of formula-1, represented by the following structur

Novel Combination Containing a Stimulator of Soluble Guanylate Cyclase and a Lipid-Lowering Substance

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Page/Page column 8, (2010/11/28)

A combination product which comprises as pharmaceutically active ingredients at least one active ingredient component A and at least one active ingredient component B, where active ingredient component A is a direct soluble guanylate cyclase stimulator of

NOVEL 2,5-DISUBSTITUTED PYRIMIDINE DERIVATIVES

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Page/Page column 28, (2010/02/06)

The invention relates to novel 2,5-disubstituted pyrimidine derivatives, which stimulate the soluble guanylate cyclase, method for production and use thereof for the production of medicaments, in particular medicaments for the treatment of central nervous system diseases.

4-AMINO-SUBSTITUTED PYRIMIDINE DERIVATIVES

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Page/Page column 20, (2010/02/06)

The invention relates to novel 4-amino-substituted pyrimidine derivatives, which stimulate soluble guanylate cyclase, method for production and use thereof for the production of medicaments, in particular medicaments for the treatment of diseases of the c

PYRIDINE-SUBSTITUTED PYRAZOLOPYRIDINE DERIVATIVE

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Page/Page column 10, (2010/02/06)

The invention relates to a substituted pyrazole derivative and the use thereof as a medicament, particularly as a medicament for treating cardiovascular diseases.

Substituted pyrazole derivatives

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Page column 31, (2010/02/09)

The present invention relates to novel substituted pyrazole derivatives of the general formula (I) in which the substituents R1, R2, R3, A, X and Y are each as defined, and to processes for their preparation and to their use as medicaments, in particular as medicaments for the treatment of cardiovascular disorders.

Novel sulfonamide-substituted pyrazolopyridine derivatives

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, (2008/06/13)

The invention relates to novel pyrazolopyridine derivatives of formula (I) wherein R1 represents H, Cl or NH2, and R2 and R3 form; together with the heteroatoms to which they are bonded, a five to six-membered heterocycle which can be saturated or partially unsaturated, can optionally contain at least one other heteroatom from the group N, O, S and can be optionally substituted. The invention also relates to salts, isomers and hydrates of said derivatives, in the form of stimulators of soluble guanylate cyclase and as agents for treating cardiovascular diseases, hypertonia, thrombo-embolic diseases and ischaemia, sexual dysfunction, inflammations, and diseases of the central nervous system.

Novel carbamate-substituted pyrazolopyridine derivatives

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, (2008/06/13)

The invention relates to novel pyrazolopyridine derivatives of the formula (I), wherein R1 represents hydrogen or a di-C1-6-alkylaminocarbonyl group, R2 represents a rest of the formula —O—CO—NR3R4, wherein R3 and R4 are the same or different and represen

Substituted pyrazole derivatives condensed with six-membered heterocyclic rings

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Page column 41, (2010/02/07)

The present invention relates to novel substituted pyrazole derivatives of the general formula (I) in which R1, R2, R3and A are each as defined, and to processes for their preparation and to their use as medicaments, in pa

Metabolites of orally active NO-independent pyrazolopyridine stimulators of soluble guanylate cyclase.

Straub, Alexander,Benet-Buckholz, Jordi,Froede, Rita,Kern, Armin,Kohlsdorfer, Christian,Schmitt, Peter,Schwarz, Thomas,Siefert, Hans Martin,Stasch, Johannes Peter

, p. 1711 - 1717 (2007/10/03)

The pyrazolopyridine stimulators of soluble guanylate cyclase BAY 41-2272 and 41-8543 were oxidised in rats and dogs at their 5-pyrimidinyl-cyclopropyl and -morpholino residue. These metabolites activate the soluble guanylate cyclase, induce vasoelaxation and thereby may contribute to the in vivo activity of BAY 41-2272 and BAY 41-8543.

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