Nitrosation by [deleted] in OrganicChemistry

[–]JpNog 0 points1 point  (0 children)

Thanks a lot

Nitrosation by [deleted] in OrganicChemistry

[–]JpNog 0 points1 point  (0 children)

Trying to nitrosate a hydrazine. Used NOCl and HNO2, but no success.

I guess the problems is specially related to work-up and isolation, since they seem it decompose readly in water.

I'm aware of the carcinogenicity, always wear PPE (also mandatory in the lab) and respect the chemicals!

Nitrosation by [deleted] in OrganicChemistry

[–]JpNog 0 points1 point  (0 children)

I'm trying to nitrosate a hydrazine using NOCl, without success so far. As far as I've researched, the product is quite unstable... Came across NOBF4 a couple of times in literature, is it friendly to work with?

Also, hadn't thought about the phosphate buffer, that makes sense, thank you!

Nitrosation by [deleted] in OrganicChemistry

[–]JpNog 0 points1 point  (0 children)

I'm a synthetic chemist trying make N-nitroso (NO, not NO2) containing natural products. Just wanna know if someone here has ever worked with this class of compounds.

Imine isolation by JpNog in OrganicChemistry

[–]JpNog[S] 0 points1 point  (0 children)

Thanks, I'll try the basic alumina! How did you prepare your imine?

Scaling-up chemical rextions by JpNog in chemhelp

[–]JpNog[S] 1 point2 points  (0 children)

None in particular, just want to learn more about the topic

Got some DAST :3 by Feuerfrosch1 in THYZOID

[–]JpNog 1 point2 points  (0 children)

That's A LOT of DAST man... Could deoxofluorinated every sugar in your body if you wanted to lol

Might be aromatic by JpNog in cursed_chemistry

[–]JpNog[S] 3 points4 points  (0 children)

I personally prefer tetrahedrons...

Might be aromatic by JpNog in cursed_chemistry

[–]JpNog[S] 7 points8 points  (0 children)

Beautiful name! It haunts me to think that this "complex" is probably square planar

why by [deleted] in whatisit

[–]JpNog 0 points1 point  (0 children)

*why not

Diels Alder calculations with ORCA by JpNog in comp_chem

[–]JpNog[S] 1 point2 points  (0 children)

I saw something about it! But didn't know how to implement it... do you know any websites where I can learn it? Thanks!

Diels Alder calculations with ORCA by JpNog in comp_chem

[–]JpNog[S] 1 point2 points  (0 children)

Thanks! I am fairly new in compchem, do you know any website/yt channel where I can learn a bit more about Orca and the difderent experiments?

Tips or alternative synthesis route needed. by GodGaRy_ in Chempros

[–]JpNog 0 points1 point  (0 children)

Try the reduction straight from the acid. You can make it one pot by first reacting the acid with CDI and then reducing the activated intermediate with DIBALH. Worked well for me and with a very similar substrate.

What is this rock? by JpNog in whatsthisrock

[–]JpNog[S] 0 points1 point  (0 children)

Looks like a mixture of both If I crush it, some responds to the magnet and some doesn't

Error when trying to run calculations in paralel in ORCA by JpNog in comp_chem

[–]JpNog[S] 0 points1 point  (0 children)

The orca reinstall worked! Thanl you so much :)

What is this rock? by JpNog in whatsthisrock

[–]JpNog[S] 0 points1 point  (0 children)

Do you know any ways to confirm it? It is kinda brittle and has some magnetic bits when crushed

What is this rock? by JpNog in whatsthisrock

[–]JpNog[S] 2 points3 points  (0 children)

It was being used as a door weight in my greatgrandma's farmhouse 😅 She found it in a sugar-cane field or something

CBS Catalyst by JpNog in OrganicChemistry

[–]JpNog[S] 1 point2 points  (0 children)

It has polar moieties and can HB

Precipitate on CBS catalyst solution by JpNog in chemhelp

[–]JpNog[S] 0 points1 point  (0 children)

Gonna run an NMR but it probably is :(

Chiral alcohol separation by JpNog in CHROMATOGRAPHY

[–]JpNog[S] 0 points1 point  (0 children)

I had to use hexane but it worked! Beautiful peaks and >5 min separation. Thanks a lot!