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1092580-91-0

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1092580-91-0 Usage

Compound type

Heterocyclic compound

Structure

Fused 6-membered pyrrolo ring and 5-membered pyridine ring

Bromine atom position

5th position

Oxygen group position

7th position

Unique chemical properties

Presence of bromine atom and oxygen group at the 7th position

Potential applications

Medicinal chemistry, pharmaceutical research, and as a building block in the synthesis of biologically active compounds

Therapeutic properties

Potential therapeutic properties due to structural features

Check Digit Verification of cas no

The CAS Registry Mumber 1092580-91-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,2,5,8 and 0 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1092580-91:
(9*1)+(8*0)+(7*9)+(6*2)+(5*5)+(4*8)+(3*0)+(2*9)+(1*1)=160
160 % 10 = 0
So 1092580-91-0 is a valid CAS Registry Number.

1092580-91-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-bromo-7-hydroxypyrrolo[2,3-b]pyridine

1.2 Other means of identification

Product number -
Other names 5-Bromo-1h-pyrrolo(2,3-b)pyridine 7-oxide

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:1092580-91-0 SDS

1092580-91-0Downstream Products

1092580-91-0Relevant articles and documents

Design and synthesis of potent RSK inhibitors

Jain, Rama,Mathur, Michelle,Lan, Jiong,Costales, Abran,Atallah, Gordana,Ramurthy, Savithri,Subramanian, Sharadha,Setti, Lina,Feucht, Paul,Warne, Bob,Doyle, Laura,Basham, Stephen,Jefferson, Anne B.,Appleton, Brent A.,Lindvall, Mika,Shafer, Cynthia M.

, p. 3197 - 3201 (2018)

Utilizing the already described 3,4-bi-aryl pyridine series as a starting point, incorporation of a second ring system with a hydrogen bond donor and additional hydrophobic contacts yielded the azaindole series which exhibited potent, picomolar RSK2 inhib

CONDENSED HETEROCYCLES AS BCL-2 INHIBITORS

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Page/Page column 264, (2021/04/10)

The disclosure includes compounds of Formula (A) wherein R1, R2, R3, R4, R5, R6, R7, R8, R9, R10, and R11, h, j, m, n, k, v, s, g, V, W, L, Z1 Q1, Q2, Q3, Q4, Q5, Q6, and Q7, are defined herein. Also disclosed is a method for treating a neoplastic disease, an autoimmune disease, or a neorodegenerative disease with these compounds.

PYRROLO[2,3-B]PYRIDINE COMPOUNDS AND THEIR USE IN THE TREATMENT OF CANCER

-

Paragraph 00153; 00164, (2019/03/05)

The present application relates to a compound of Formula I, or a salt, hydrate or solvate thereof, as defined herein. The present compounds are found to have pharmacological effects, particularly at MRCK. Further provided are pharmaceutical compositions comprising said compounds. The present invention also relates to the use of these compounds as therapeutic agents, in particular, for the treatment and/or prevention of proliferative diseases, such as cancer.

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