CS Support Forum - Safari Problem

Alan Gorman commented in my last post that the support staff at CambridgeSoft can find no problems accessing their support forums from Safari. I, on the other hand, have a completely different experience. I have made a video demonstrating the problems with their forums. This was recorded using Safari 5.0.1 on Mac OS 10.5.8 Leopard. I have tried on four different macs and the same problem occurs on all of them using Leopard or Snow Leopard.

One issue that you will see at the beginning is a problem with the first link on their support site. I can get that far if I am not logged in but accessing it as a guest. However, once I enter my login information the support forum web page simply will not load in Safari. Thinking this was a cookie problem I checked my settings. Even at the least secure setting to always accept cookies the error results.

I should note that the same server problem with the first link occurs in Firefox 3.5.11 as well. When I log in I get a similar error that says the page is not redirecting properly. "Firefox has detected that the server is redirecting the request for this address in a way that will never complete."

ACS Blogging - Cambridgesoft

As I was wandering through the expo this morning trying to dry off after a soaking walk from my hotel, I stopped by the Cambridgesoft booth to chat about their Mac products excuses for software. It was very clear after inquiring about their development that they have no interest in trying to improve the Mac software. All I got was excuse after excuse about how we are only 5% of their clients and we really aren't worth investing in. Cambridgesoft is clearly a follower and not a leader when it comes to software development. They will only invest in their products if they are absolutely guaranteed to make a lot of money. What a pity. If they had this attitude when the company first started, they would not exist today. They still keep blaming all of the problems on Apple and Microsoft. Not that those companies don't share responsibility for the bugs. I guess it's time to give ChemDoodle a good trial. If i can get over the learning curve, it looks like the best solution for chemistry drawing on a Mac anytime soon.

Update: After lunch I returned to the expo and happened to bump into some of the McGraw Hill folks at the CambridgeSoft booth. They were showing their upcoming educational tools combining Connect with a ChemDraw plugin and Blackboard interface. This product looks very promising. Anyway, I got pulled back into some lengthy conversations. I do want to set the record straight. My rant above is all about CambridgeSoft's Mac support. Their windows products are actually quite good and improving all the time. Although I stand behind my statement that this company is a follower and not an innovator, I understand the economics of business. It is our job to let the company know that the market demand is out there. So, if all you pharmaceutical companies would just switch over to Macs and ask CambridgeSoft to start delivering their software to you, I would really appreciate it. And CambridgeSoft, I want to say please don't underestimate the growing Mac market. Frankly if you would just focus on making ChemDraw work well we would be ecstatic. And if you could make a simple Chem drawing app for the iPad that would be the icing on the cake!

ACS Liveblogging Sunday Morning

10:50 am Arrived a little late this morning. I know it is only Sunday morning, but the Boston convention center seems quite dead. It took me 20 minutes just to find the one coffee cart that was open. I will be looking for the Keith Fagnou memorial symposium soon. I missed Hartwig, Sanford and Yu. Jacobson is the last speaker. I'll try to catch some of his talk.

11:15 am Jacobson is talking up reaction calorimetry for kinetic analysis. Not really new but I suppose organic chemists haven't utilized this great technique.

11:26 am Some nice new insight into the Co-salen catalyzed epoxide hydrolysis being presented. It seems using a tosylate counter ion on the cobalt is very different from Cl or OAc. The rate doesn't seem to slow down but expoxide opening is very reversible due to the good leaving group ability of tosylate. This leads to racemization and poor kinetic resolution.

11:40 am Jacobson appears to be flustered today. He's stumbling over words and seems unsure of his slides. Never the less he still has great science to share. It appears that chirality on both the activated epoxide electrophile and the Co-OH nucleophile are important for kinetic resolution. Enantioselectivity is not dependent on the chiral backbone as the ligand complex forms the same stepped configuration of the arylation groups of the salen regardless of the backbone. It is only necessary that backbone allows them to have the same sense of chirality.

11:50 am Ooh. Cyclic oligomers of the salen ligand with local C2 symmetry. Very efficient HKR at only 0.001 mol% loading. Salens connected with ether linkages. Rate is much improved over the monomeric catalyst.

Boston or Bust

I am heading to Boston today for a few days at the ACS meeting. If I see anything worth reporting, I'll share it here. That being said, I usually find myself at ACS meetings not attending as many talks as I would like but instead networking with friends and acquaintances. I am looking forward to some good dining experiences!

Carbon Tetrachloride

Who could not feel sorry for this much maligned molecule. Simple in its structure but so complex in its properties. It is a nonpolar solvent that is still the best for bromination chemistry. Sure it has its environmental issues and has largely been replaced but it will never go away completely. More about the history of carbon tet in a minute. Let's talk about this blog for a moment. Many people think I named this blog after tetrachloromethane. I suppose that was one aspect of the name that appealed to me but it really was much more than that. There is more to Carbon Tet than the halomethane. I thought the name could also connote 'Tetrahedral Carbon' which would play right into the topics of asymmetric synthesis and catalysis. And, besides, I just like saying 'Carbon Tet! Carbon Tet!'.

But this is a chemistry blog, so let's talk a bit more about the molecule. Carbon tet was first prepared way back in 1839. The French chemist Henri Victor Regnault reacted chloroform with chlorine producing carbon tet and HCl. Now it is made from methane but before the 1950s it was prepared by chlorination of carbon disulfide.

As a halocarbon it is not flammable. In the early part of the 20th century carbon tetrachloride was used to extinguish fires. It was placed into brass bottles with a pump which was used to spray carbon tet onto a fire. If you tour some of the mansions of Newport, RI you may find some of the historic homes had vessels of carbon tet mounted near the ceiling. In the case of a fire the contents would spill out into the room to help douse the fire. It was also used as a dry cleaning solvent as it is particularly good at dissolving nonpolar grease.

Since the 1980s production of carbon tetrachloride has dropped precipitously due to its role in the destruction of the ozone layer. Industry has all but abandoned its use though it is still used in small quantities for research purposes. Once a cheap solvent, carbon tet now costs more than gold. If you have any, hang on to it! It could be your hedge against inflation.

The Demise of the Chemistry Blog

Blogs come and blogs go. I know that. Mine has been defunct for almost two years. But so have many other chemistry blogs that I used to have in my blog list. Some have stopped blogging, some have joined forces with other blogs and some have just disappeared completely. I went through my blog list and pulled out all of the defunct blogs. I don't want Carbon Tet to be included in this list! I wonder if any of these blogs will wake back up? Regardless, CT is alive. Stay Tuned!

Defunct Chemistry Blogs

A Synthetic Environment
Atom Pushers Anonymous

Chem Blog
ChemBark
Chemical Musings
Chemist in a Transition State
jungfreudlich.de
Liquid Carbon
Totally Mechanistic
Totally Medicinal
Two-Headed Chemical Mayhem
Whistling in the Wind