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78593-33-6

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78593-33-6 Usage

General Description

3-bromocinnoline is an organic compound with the chemical formula C9H6BrN. It is a brominated derivative of cinnoline, containing a bromine atom attached to the third position of the cinnoline ring. 3-bromocinnoline is a light yellow solid that is insoluble in water but soluble in organic solvents. It is used as a building block in organic synthesis and chemical reactions due to its unique structure and reactivity. 3-bromocinnoline is also used in the pharmaceutical industry for the synthesis of various drugs and as a reagent in research laboratories. Its properties and potential applications make 3-bromocinnoline an important and versatile chemical compound in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 78593-33-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,5,9 and 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 78593-33:
(7*7)+(6*8)+(5*5)+(4*9)+(3*3)+(2*3)+(1*3)=176
176 % 10 = 6
So 78593-33-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H5BrN2/c9-8-5-6-3-1-2-4-7(6)10-11-8/h1-5H

78593-33-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Bromocinnoline

1.2 Other means of identification

Product number -
Other names 3-bromocinnoline

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:78593-33-6 SDS

78593-33-6Relevant articles and documents

TMP-magnesium and TMP-Zinc bases for the regioselective metalation of the cinnoline scaffold

Klatt, Thomas,Roman, Daniela Sustac,Leon, Thierry,Knochel, Paul

supporting information, p. 1232 - 1235 (2014/03/21)

A regioselective functionalization of cinnolines in positions 3 and 8 using metalations has been developed. This involves either the use of a frustrated Lewis pair consisting of BF3·Et2O and TMP 2Mg·2LiCl or the in situ generated base TMP 2Zn·2MgCl2·2LiCl. Successive metalations allow the preparation of 3,8-disubstituted cinnolines. Various functionalizations by acylation, allylation, and cross-coupling reactions with aryl halides or alkenyl iodides were carried out successfully.

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