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N-(1)-BOC-5-NITRO-INDAZOLE is a chemical compound that features a BOC (tert-butoxycarbonyl) protecting group and a nitro group attached to an indazole ring. The BOC group is commonly utilized in organic synthesis to shield amines, while the nitro group is recognized for its electron-withdrawing characteristics. Indazoles, being heterocyclic aromatic compounds, have been instrumental in the development of pharmaceuticals and agrochemicals. The incorporation of the BOC and nitro groups in N-(1)-BOC-5-NITRO-INDAZOLE renders it a significant intermediate for the synthesis of various indazole-based compounds, which hold potential applications in the fields of medicine and agriculture. Its distinctive structural attributes and reactivity position it as a valuable building block for the creation of a wide array of chemical compounds.

129488-09-1

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129488-09-1 Usage

Uses

Used in Pharmaceutical Chemistry:
N-(1)-BOC-5-NITRO-INDAZOLE is used as a key intermediate in the synthesis of pharmaceutical compounds for its ability to be further modified and functionalized to create new drug candidates. Its presence in the molecule allows for the development of potential therapeutic agents that can be tailored to target specific biological pathways or receptors.
Used in Agrochemical Development:
In the agrochemical industry, N-(1)-BOC-5-NITRO-INDAZOLE is used as a precursor in the creation of new pesticides or herbicides. N-(1)-BOC-5-NITRO-INDAZOLE's reactivity and structural features enable the design of molecules that can effectively control or eliminate unwanted plant species or pests, thereby enhancing crop yields and quality.
Used in Organic Synthesis:
N-(1)-BOC-5-NITRO-INDAZOLE is utilized as a versatile building block in organic synthesis for its potential to be transformed into a range of different chemical entities. The BOC protecting group can be selectively removed under mild conditions, unveiling the amine functionality for further reactions, while the nitro group can be reduced or otherwise modified to introduce various functional groups.
Used in Research and Development:
In academic and industrial research settings, N-(1)-BOC-5-NITRO-INDAZOLE serves as a valuable tool for exploring new chemical reactions and mechanisms. Its unique properties can provide insights into the reactivity of related compounds and contribute to the advancement of synthetic methodologies.

Check Digit Verification of cas no

The CAS Registry Mumber 129488-09-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,4,8 and 8 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 129488-09:
(8*1)+(7*2)+(6*9)+(5*4)+(4*8)+(3*8)+(2*0)+(1*9)=161
161 % 10 = 1
So 129488-09-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H13N3O4/c1-12(2,3)19-11(16)14-10-5-4-9(15(17)18)6-8(10)7-13-14/h4-7H,1-3H3

129488-09-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 5-nitroindazole-1-carboxylate

1.2 Other means of identification

Product number -
Other names 5-nitro-indazole-1-carboxylic acid t-butyl ester

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:129488-09-1 SDS

129488-09-1Relevant articles and documents

Synthesis of novel N-Aryl-1H-indazolamines from amino-1H-indazoles and arylboronic acids

Swamy, Udutha Kumara,Mohan, H. Rama,Prasad, U. Viplava

, p. 7539 - 7543 (2014)

An efficient and high-yielding synthesis of N-aryl-1H-indazolamines from amino-1H-indazole and arylboronic acids are described. In this study a series of novel N-aryl-1H-indazolamines (1a-i) were synthesized using arylboronic acids and amino-1 H-indazoles

EP300/CREBBP INHIBITOR

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Paragraph 0206; 0207, (2020/05/30)

The present invention provides a compound having excellent histone acetyltransferase inhibitory activity against EP300 and/or CREBBP, or a pharmacologically acceptable salt thereof. The compound is represented by the following formula (1) or a pharmacologically acceptable salt thereof: wherein ring Q1, ring Q2, R1, R2, R3 and R4 respectively have the same meanings as defined in the specification.

RHO-ASSOCIATED PROTEIN KINASE INHIBITOR, PHARMACEUTICAL COMPOSITION COMPRISING THE SAME, AS WELL AS PREPARATION METHOD AND USE THEREOF

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Paragraph 0104; 0105, (2019/01/11)

The present invention relates to a Rho-associated protein kinase inhibitor of Formula (I), a pharmaceutical composition comprising the same, a preparation method thereof, and use thereof for the prevention or treatment of a disease mediated by the Rho-associated protein kinase (ROCK).

RHO-ASSOCIATED PROTEIN KINASE INHIBITOR, PHARMACEUTICAL COMPOSITION COMPRISING THE SAME, AS WELL AS PREPARATION METHOD AND USE THEREOF

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Paragraph 0102; 0103, (2019/01/11)

The present invention relates to a Rho-associated protein kinase inhibitor of Formula (I), a pharmaceutical composition comprising the same, a preparation method thereof, and use thereof for the prevention or treatment of a disease mediated by the Rho-associated protein kinase (ROCK).

HEPARAN SULFATE BIOSYNTHESIS INHIBITORS FOR THE TREATMENT OF DISEASES

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Paragraph 000370, (2016/05/02)

Described herein are compounds of Formula I, methods of making such compounds, pharmaceutical compositions and medicaments containing such compounds, and methods of using such compounds to treat or prevent diseases or conditions in need of inhibition of heparan sulfate biosynthesis.

NOVEL ROCK INHIBITORS

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Paragraph 0327-0328, (2014/03/24)

The present invention relates to new kinase inhibitors of Formula (I), wherein X is oxygen, —NH—, or a direct bond; Y is —NH— or a direct bond; n is an integer from 0 to 4; m is an integer from 0 to 4; Cy represents a bivalent radical consisting of a satured (poly)cycle, including fused, bi-, spiro or bridged carbocycles and heterocycles; in particular selected from the group consisting of: Formula (II), Ar is selected from the group comprising: Formula (III), R2 is hydrogen or methyl; R8 is hydrogen, methyl, halogen, or alkynyl; R1 is an aryl or heteroaryl more specifically ROCK inhibitors, compositions, in particular pharmaceuticals, comprising such inhibitors, and to uses of such inhibitors in the treatment and prophylaxis of disease. In particular, the present invention relates to new ROCK inhibitors, compositions, in particular pharmaceuticals, comprising such inhibitors, and to uses of such inhibitors in the treatment and prophylaxis of disease. In addition, the invention relates to methods of treatment and use of said compounds in the manufacture of a medicament for the application to a number of therapeutic indications including sexual dysfunction, inflammatory diseases, ophthalmic diseases and Respiratory diseases.

NOVEL ROCK INHIBITORS

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Page/Page column 36, (2014/05/24)

The present invention relates to new kinase inhibitors, more specifically ROCK inhibitors, compositions, in particular pharmaceuticals, comprising such inhibitors, and to uses of such inhibitors in the treatment and prophylaxis of disease. In particular, the present invention relates to new ROCK inhibitors, compositions, in particular pharmaceutic-als, comprising such inhibitors, and to uses of such inhibitors in the treatment and prophylaxis of disease. In addition, the invention relates to methods of treatment and use of said compounds in the manufacture of a medicament for the ap-plication to a number of therapeutic indications including sexual dysfunction, inflammatory diseases, ophthalmic dis-eases and Respiratory diseases. Compounds of the invention display soft drug characteristics, i.e. they are rapidly inactivated upon entry in the systemic circulation. Therefore, they allow for reduced systemic exposure to functionally active ROCK inhibitors

NOVEL ROCK INHIBITORS

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Page/Page column 47, (2012/11/13)

The present invention relates to new kinase inhibitors, more specifically ROCK inhibitors, compositions, in particular pharmaceuticals, comprising such inhibitors, and to uses of such inhibitors in the treatment and prophylaxis of disease. In particular, the present invention relates to new ROCK inhibitors, compositions, in particular pharmaceuticals, comprising such inhibitors, and to uses of such inhibitors in the treatment and prophylaxis of disease. In addition, the invention relates to methods of treatment and use of said compounds in the manufacture of a medicament for the application to a number of therapeutic indications including sexual dysfunction, inflammatory diseases, ophthalmic diseases and Respiratory diseases.

QUINAZOLINONE AND FUSED PYRIMIDINONE COMPOUNDS AND THEIR USE IN TREATING SODIUM CHANNEL-MEDIATED DISEASES OR CONDITIONS

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Page/Page column 98-99, (2008/12/07)

This invention is directed to compounds of formula (I): wherein (A), n, R1, R2 and R3 are as defined herein, as a stereoisomer, enantiomer, tautomer thereof or mixtures thereof; or a pharmaceutically acceptable salt, solvate or prodrug thereof, for the treatment and/or prevention of sodium channel-mediated diseases or conditions, such as pain.

N-ureidoheterocycloalkyl-piperidines as modulators of chemokine receptor activity

-

, (2008/06/13)

The present application describes modulators of CCR3 of formula (I): or pharmaceutically acceptable salt forms thereof, useful for the prevention of asthma and other allergic diseases.

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