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1-Boc-3-bromo-5-azaindole is a chemical compound with the molecular formula C12H13BrN2O2, characterized by its unique structure as a derivative of 5-azaindole, a heterocyclic compound. The "1-Boc" in its name signifies the presence of a tert-butoxycarbonyl (Boc) protecting group on the nitrogen atom of the indole ring, while the "3-bromo" denotes a bromine atom at the 3 position on the indole ring. 1-Boc-3-bromo-5-azaindole is recognized for its role as a building block in the synthesis of pharmaceuticals and other organic compounds, and it is particularly valuable in the field of medicinal chemistry for the development of new drugs due to its distinctive structure and reactivity.

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  • 192189-16-5 Structure
  • Basic information

    1. Product Name: 1-Boc-3-bromo-5-azaindole
    2. Synonyms: 1-Boc-3-bromo-5-azaindole;tert-butyl 3-bromo-1H-pyrrolo[3,2-c]pyridine-1-carboxylate
    3. CAS NO:192189-16-5
    4. Molecular Formula: C12H13BrN2O2
    5. Molecular Weight: 297.14782
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 192189-16-5.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.: Sealed in dry,Room Temperature
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-Boc-3-bromo-5-azaindole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-Boc-3-bromo-5-azaindole(192189-16-5)
    11. EPA Substance Registry System: 1-Boc-3-bromo-5-azaindole(192189-16-5)
  • 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: 192189-16-5(Hazardous Substances Data)

192189-16-5 Usage

Uses

Used in Pharmaceutical Synthesis:
1-Boc-3-bromo-5-azaindole is used as a key building block for the synthesis of pharmaceuticals, contributing to the creation of a wide range of organic compounds. Its presence of a Boc protecting group and a bromine atom at a strategic position on the indole ring facilitates various chemical reactions, making it a versatile component in the development of new drugs.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 1-Boc-3-bromo-5-azaindole is utilized as a valuable tool for the development of novel drugs. Its unique structure and reactivity allow for the preparation of diverse chemical compounds, which can be further modified and optimized for specific therapeutic applications, enhancing the discovery and design of new pharmaceutical agents.

Check Digit Verification of cas no

The CAS Registry Mumber 192189-16-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,2,1,8 and 9 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 192189-16:
(8*1)+(7*9)+(6*2)+(5*1)+(4*8)+(3*9)+(2*1)+(1*6)=155
155 % 10 = 5
So 192189-16-5 is a valid CAS Registry Number.

192189-16-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 3-bromopyrrolo[3,2-c]pyridine-1-carboxylate

1.2 Other means of identification

Product number -
Other names C-8017

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:192189-16-5 SDS

192189-16-5Relevant articles and documents

New Enzyme Inhibitor Compounds

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Paragraph 0183; 0184, (2013/05/08)

Disclosed are compounds which inhibit SSAO enzyme activity. Also disclosed are pharmaceutical compositions comprising these compounds and the use of these compounds in the treatment or prevention of medical conditions wherein inhibition of SSAO activity is beneficial, such as inflammatory diseases, immune disorders and the inhibition of tumour growth.

NEW ENZYME INHIBITOR COMPOUNDS

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Page/Page column 35, (2011/10/10)

Compounds of formula (I) are inhibitors of Semicarbazide-sensitive amine oxidase wherein R1, A, X and R2 are as defined in the claims.

5-AZAINDOLE BISPHOSPHONATES

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Page/Page column 28, (2010/04/25)

Novel 5-azaindole bisphosphonate compounds are disclosed, as well as methods of preparing the compounds, pharmaceutical compositions including the compounds, and administration of the compounds in methods of treating abnormal calcium and phosphate metabolism, including bone and joint diseases and other disorders.

Novel non-nucleoside inhibitors of human immunodeficiency virus type 1 reverse transcriptase. 6. 2-Indol-3-yl- and 2-azaindol-3-yl- dipyridodiazepinones

Kelly,McNeil,Rose,David,Shih,Grob

, p. 2430 - 2433 (2007/10/03)

Modification of the non-nucleoside inhibitor of HIV-1 reverse transcriptase nevirapine (Viramune) by incorporation of a 2-indolyl substituent confers activity against several mutant forms of the enzyme.

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