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1086389-94-7

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1086389-94-7 Usage

General Description

3,5-DibroMo-1H-pyrrolo[2,3-b]pyridine is a chemical compound with the molecular formula C7H4Br2N2. It is a brominated heterocyclic compound consisting of a pyrrolopyridine ring system. 3,5-DibroMo-1H-pyrrolo[2,3-b]pyridine has potential applications in the field of pharmaceuticals and agrochemicals due to its unique structure and properties. It may also be used as a building block in organic synthesis to create more complex molecules. Additionally, it is important to handle this compound with care as it may have potential health and environmental hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 1086389-94-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,8,6,3,8 and 9 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1086389-94:
(9*1)+(8*0)+(7*8)+(6*6)+(5*3)+(4*8)+(3*9)+(2*9)+(1*4)=197
197 % 10 = 7
So 1086389-94-7 is a valid CAS Registry Number.

1086389-94-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-Dibromo-1H-pyrrolo[2,3-b]pyridine

1.2 Other means of identification

Product number -
Other names 2,5-dibromo-1H-pyrrolo[2,3-b]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:1086389-94-7 SDS

1086389-94-7Downstream Products

1086389-94-7Relevant articles and documents

Regioselective Halogenation of Arenes and Heterocycles in Hexafluoroisopropanol

Tang, Ren-Jin,Milcent, Thierry,Crousse, Benoit

, p. 930 - 938 (2018/01/28)

Regioselective halogenation of arenes and heterocycles with N-halosuccinimides in fluorinated alcohols is disclosed. Under mild condition reactions, a wide diversity of halogenated arenes are obtained in good yields with high regioselectivity. Additionally, the versatility of the method is demonstrated by the development of one-pot sequential halogenation and halogenation-Suzuki cross-coupling reactions.

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