Welcome to LookChem.com Sign In|Join Free
  • or
3-BROMO-1H-PYRROLO[2,3-C]PYRIDINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67058-76-8

Post Buying Request

67058-76-8 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

67058-76-8 Usage

Uses

3-Bromo-1H-pyrrolo[2,3-c]pyridine is a useful reactant for regioselective halogenation.

Check Digit Verification of cas no

The CAS Registry Mumber 67058-76-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,0,5 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 67058-76:
(7*6)+(6*7)+(5*0)+(4*5)+(3*8)+(2*7)+(1*6)=148
148 % 10 = 8
So 67058-76-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H5BrN2/c8-6-3-10-7-4-9-2-1-5(6)7/h1-4,10H

67058-76-8SDS

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 3-Bromo-1H-pyrrolo[2,3-c]pyridine

1.2 Other means of identification

Product number -
Other names 3-bromo-1H-pyrrolo[2,3-c]pyridine

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:67058-76-8 SDS

67058-76-8Upstream product

67058-76-8Relevant academic research and scientific papers

Regioselective halogenation of 6-azaindoles: Efficient synthesis of 3-halo-2,3-disubstituted-6-azaindole derivatives

Gallou, Fabrice,Reeves, Jonathan T.,Tan, Zhulin,Song, Jinhua J.,Yee, Nathan K.,Campbell, Scot,Jones, Paul-James,Senanayake, Chris H.

, p. 2400 - 2402 (2005)

A mild and efficient synthesis of 3-halo-2-substituted-6-azaindoles was developed by regioselective halogenation of 6-azaindole systems. The transformation was achieved with copper(II) bromide in acetonitrile at room temperature. Georg Thieme Verlag Stutt

PIM KINASE INHIBITOR COMPOSITIONS AND USES THEREOF

-

Paragraph 0233, (2020/11/12)

This disclosure relates to compounds and compositions useful as inhibitors of PIM kinases. Also provided are methods of synthesis and methods of use of PIM inhibitors in treating individuals suffering from cancerous malignancies.

Discovery and optimization of a novel series of dyrk1b kinase inhibitors to explore a MEK resistance hypothesis

Kettle, Jason G.,Ballard, Peter,Bardelle, Catherine,Cockerill, Mark,Colclough, Nicola,Critchlow, Susan E.,Debreczeni, Judit,Fairley, Gary,Fillery, Shaun,Graham, Mark A.,Goodwin, Louise,Guichard, Sylvie,Hudson, Kevin,Ward, Richard A.,Whittaker, David

, p. 2834 - 2844 (2015/04/14)

Potent and selective inhibitors of Dyrk1B kinase were developed to explore the hypothesis, based on siRNA studies, that Dyrk1B may be a resistance mechanism in cells undergoing a stress response.

Practical regioselective bromination of azaindoles and diazaindoles

Gallou, Fabrice,Reeves, Jonathan T.,Tan, Zhulin,Song, Jinhua J.,Yee, Nathan K.,Harcken, Christian,Liu, Pingrong,Thomson, David,Senanayake, Chris H.

, p. 211 - 214 (2007/10/03)

A mild and efficient synthesis of various 3-brominated azaindoles and diazaindoles was developed by regioselective halogenation of the parent systems. This practical and high-yielding transformation was achieved with copper(II) bromide in acetonitrile at

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.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 67058-76-8