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1-(2-Fluorobenzyl)-1H-pyrazolo[3,4-b]pyridine-3-carboxylic acid ethyl ester is a complex organic compound characterized by its unique molecular structure. It is a derivative of pyrazolo[3,4-b]pyridine with a fluorobenzyl group attached to the first position and an ethyl ester group at the third position of the carboxylic acid. 1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridine-3-carboxylic acid ethyl ester has been the subject of various research studies due to its potential applications in different fields.

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  • 1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridine-3-carboxylic acid ethyl ester

    Cas No: 256376-59-7

  • USD $ 1.9-2.9 / Gram

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  • 256376-59-7 Structure
  • Basic information

    1. Product Name: 1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridine-3-carboxylic acid ethyl ester
    2. Synonyms: 1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridine-3-carboxylic acid ethyl ester;Ethyl 1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridine-3-carboxylate
    3. CAS NO:256376-59-7
    4. Molecular Formula: C16H14FN3O2
    5. Molecular Weight: 299.2996632
    6. EINECS: -0
    7. Product Categories: N/A
    8. Mol File: 256376-59-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: Refrigerator
    8. Solubility: DMSO (Slightly), Methanol (Very Silghtly)
    9. CAS DataBase Reference: 1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridine-3-carboxylic acid ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridine-3-carboxylic acid ethyl ester(256376-59-7)
    11. EPA Substance Registry System: 1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridine-3-carboxylic acid ethyl ester(256376-59-7)
  • 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: 256376-59-7(Hazardous Substances Data)

256376-59-7 Usage

Uses

1. Used in Pharmaceutical Research:
1-(2-Fluorobenzyl)-1H-pyrazolo[3,4-b]pyridine-3-carboxylic acid ethyl ester is used as a stimulator of soluble guanylate cyclase for the development of novel therapeutic agents. Soluble guanylate cyclase is an enzyme that plays a crucial role in the regulation of vascular tone, blood flow, and blood pressure. By stimulating this enzyme, the compound may have potential applications in the treatment of various cardiovascular diseases and conditions related to nitric oxide signaling.
2. Used in Chemical Synthesis:
1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridine-3-carboxylic acid ethyl ester can also be utilized as an intermediate or building block in the synthesis of more complex molecules with potential pharmaceutical or chemical applications. Its unique structure and functional groups make it a valuable candidate for further modification and development of new compounds with specific properties and activities.
3. Used in Academic Research:
1-(2-Fluorobenzyl)-1H-pyrazolo[3,4-b]pyridine-3-carboxylic acid ethyl ester serves as a subject of interest in academic research, where scientists investigate its chemical properties, reactivity, and potential interactions with biological targets. This research can contribute to the understanding of the compound's mechanisms of action and its potential applications in various fields, including drug discovery and development.

Check Digit Verification of cas no

The CAS Registry Mumber 256376-59-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,6,3,7 and 6 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 256376-59:
(8*2)+(7*5)+(6*6)+(5*3)+(4*7)+(3*6)+(2*5)+(1*9)=167
167 % 10 = 7
So 256376-59-7 is a valid CAS Registry Number.

256376-59-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridine-3-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl 3-[1-(3-carbethoxy)-piperidinyl]propionate

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:256376-59-7 SDS

256376-59-7Relevant 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 32; 33; 42, (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 8-9, (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

4-AMINO-SUBSTITUTED PYRIMIDINE DERIVATIVES

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Page/Page column 21, (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 11, (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.

NOVEL 2,5-DISUBSTITUTED PYRIMIDINE DERIVATIVES

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Page/Page column 28-29, (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.

Substituted pyrazole derivatives

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Page column 32, (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.

Substituted pyrazole derivatives condensed with six-membered heterocyclic rings

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Page column 41-42, (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

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

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