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128780-26-7

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128780-26-7 Usage

Description

Bicyclo[2.2.1]hepta-2,5-diene, 2-bromo-3-chlorois a chemical compound with the molecular formula C7H7BrCl. It is a bicyclic compound, containing a seven-membered ring with two double bonds and substituents of bromine and chlorine. Its unique structure and reactivity make it an important building block for the synthesis of complex organic molecules.

Uses

Used in Pharmaceutical Industry:
Bicyclo[2.2.1]hepta-2,5-diene, 2-bromo-3-chlorois used as a synthetic intermediate for the production of pharmaceuticals. Its unique structure and reactivity allow for the synthesis of complex organic molecules, making it a valuable component in the development of new drugs.
Used in Agrochemical Industry:
Bicyclo[2.2.1]hepta-2,5-diene, 2-bromo-3-chlorois also used as a synthetic intermediate in the production of agrochemicals. Its versatility in organic synthesis enables the creation of various agrochemical compounds, contributing to the development of effective crop protection products.
It is important to handle Bicyclo[2.2.1]hepta-2,5-diene, 2-bromo-3-chlorowith caution as it has potential health hazards and should be used in a controlled environment.

Check Digit Verification of cas no

The CAS Registry Mumber 128780-26-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,7,8 and 0 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 128780-26:
(8*1)+(7*2)+(6*8)+(5*7)+(4*8)+(3*0)+(2*2)+(1*6)=147
147 % 10 = 7
So 128780-26-7 is a valid CAS Registry Number.

128780-26-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-bromo-2-chlorobicyclo[2.2.1]hepta-2,5-diene

1.2 Other means of identification

Product number -
Other names 2-chloro-3-bromo-norbornadiene

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:128780-26-7 SDS

128780-26-7Relevant articles and documents

Synthesis of 2,3-disubstituted norbornadienes

Tranmer, Geoffrey K.,Yip, Carol,Handerson, Sean,Jordan, Robert W.,Tam, William

, p. 527 - 535 (2000)

Various 2,3-disubstituted norbornadienes that can hardly be made by the traditional Diels-Alder method were synthesized by double lithium halide exchange of 2,3-dibromonorbornadiene in moderate to good yields.

Norbornadiene-bridged diarylethenes and their conversion into turn-off fluorescent photoswitches

Büllmann, Simon M.,J?schke, Andres

, p. 7124 - 7127 (2020/07/14)

We describe the synthesis and characterization of novel diarylethene photoswitches that contain a norbornadiene bridge and operate as p-type positive photochromes. One of the double bonds of norbornadiene is furthermore utilized to attach a fluoresceine tetrazine by an iEDDA cascade reaction, thereby forming a turn-off mode fluorescent photoswitch. This journal is

Enantiomeric discrimination in a reiterative domino coupling process: CuI-mediated Syn cyclotrimerization of racemic polycyclic trimethylstannyl bromonorbornadienes

Cossu, Sergio,Cimenti, Chiara,Peluso, Paola,Paulon, Antonio,De Lucchi, Ottorino

, p. 4086 - 4089 (2007/10/03)

The challenge to generate all-syn architecture has prompted the synthesis of syn cyclotrimers 2 from racemic bromotrimethylstannyl polycyclic alkenes 1. The syn-selective CuI-catalyzed cyclotrimerization process is both regio- and chemo-selective.

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