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107164-93-2

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107164-93-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107164-93-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,1,6 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 107164-93:
(8*1)+(7*0)+(6*7)+(5*1)+(4*6)+(3*4)+(2*9)+(1*3)=112
112 % 10 = 2
So 107164-93-2 is a valid CAS Registry Number.

107164-93-2SDS

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 1,3-bis(bromomethyl)-5-iodobenzene

1.2 Other means of identification

Product number -
Other names 3,5-di(bromomethyl)-iodobenzene

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:107164-93-2 SDS

107164-93-2Relevant articles and documents

Acceleration of CO2 insertion into metal hydrides: Ligand, Lewis acid, and solvent effects on reaction kinetics

Heimann, Jessica E.,Bernskoetter, Wesley H.,Hazari, Nilay,Mayer, James M.

, p. 6629 - 6638 (2018)

The insertion of CO2 into metal hydrides and the microscopic reverse decarboxylation of metal formates are important elementary steps in catalytic cycles for both CO2 hydrogenation to formic acid and methanol as well as formic acid and methanol dehydrogenation. Here, we use rapid mixing stopped-flow techniques to study the kinetics and mechanism of CO2 insertion into transition metal hydrides. The investigation finds that the most effective method to accelerate the rate of CO2 insertion into a metal hydride can be dependent on the nature of the rate-determining transition state (TS). We demonstrate that for an innersphere CO2 insertion reaction, which is proposed to have a direct interaction between CO2 and the metal in the rate-determining TS, the rate of insertion increases as the ancillary ligand becomes more electron rich or less sterically bulky. There is, however, no rate enhancement from Lewis acids (LA). In comparison, we establish that for an outersphere CO2 insertion, proposed to proceed with no interaction between CO2 and the metal in the rate-determining TS, there is a dramatic LA effect. Furthermore, for both inner- and outersphere reactions, we show that there is a small solvent effect on the rate of CO2 insertion. Solvents that have higher acceptor numbers generally lead to faster CO2 insertion. Our results provide an experimental method to determine the pathway for CO2 insertion and offer guidance for rate enhancement in CO2 reduction catalysis.

POLYCYCLIC COMPOUNDS AND METHODS OF MAKING AND USING THE SAME

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Page/Page column 163; 165, (2014/07/07)

The present disclosure provides compounds, or pharmaceutically acceptable salts thereof, for inhibiting the growth of a microbe; treating a mammal having a microbial infection, malaria, mucositis, an ophthalmic infection, an otic infection, a cancer, or a Mycobacterium infection; killing or inhibiting the growth of a Plasmodium species; inhibiting the growth of a Mycobacterium species; modulating an immune response in a mammal; or antagonizing unfractionated heparin, low molecular weight heparin, or a heparin/low molecular weight heparin derivative.

Synthesis and properties of carborane-appended C3-symmetrical extended π systems

Dash, Barada Prasanna,Satapathy, Rashmirekha,Gaillard, Elizabeth R.,Maguire, John A.,Hosmane, Narayan S.

scheme or table, p. 6578 - 6587 (2010/07/03)

A series of C3-symmetric π-conjugated compounds containing three to six o-carborane clusters have been synthesized by employing palladium-catalyzed Suzuki coupling reactions and palladium-catalyzed acetylation reactions, followed by silicon tet

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