(R)-1-([1,2,4]triazolo[4,3-a]pyridin-3-yl)ethanamine

Base Information

Chemical Name:(R)-1-([1,2,4]triazolo[4,3-a]pyridin-3-yl)ethanamine
CAS No.:1217810-82-6
Molecular Formula:C8 H10N4
Molecular Weight:162
Hs Code.:2933990090
DSSTox Substance ID:DTXSID50429242
Wikidata:Q72491799
Mol file:1217810-82-6.mol

Synonyms:(R)-1-([1,2,4]triazolo[4,3-a]pyridin-3-yl)ethanamine;1217810-82-6;(1R)-1-([1,2,4]triazolo[4,3-a]pyridin-3-yl)ethanamine;DTXSID50429242;FQWYAIRHWCMQNP-ZCFIWIBFSA-N;AKOS016844079;(R)-1-([1,2,4]triazolo[4,3-a]pyridin-3-yl)ethan-1-amine

Suppliers and Price of (R)-1-([1,2,4]triazolo[4,3-a]pyridin-3-yl)ethanamine

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Crysdot
(R)-1-([1,2,4]Triazolo[4,3-a]pyridin-3-yl)ethanamine 95+%
1g
$ 772.00

Alichem
(R)-1-([1,2,4]Triazolo[4,3-a]pyridin-3-yl)ethanamine
1g
$ 665.68

Total 4 raw suppliers

Chemical Property of (R)-1-([1,2,4]triazolo[4,3-a]pyridin-3-yl)ethanamine

Chemical Property:

PSA：56.21000
Density:1.34
LogP:1.44930
Storage Temp.:2-8°C
XLogP3:0.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:162.090546336
Heavy Atom Count:12
Complexity:161

Purity/Quality:

≥99% ^*data from raw suppliers

(R)-1-([1,2,4]Triazolo[4,3-a]pyridin-3-yl)ethanamine 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C1=NN=C2N1C=CC=C2)N
Isomeric SMILES:C[C@H](C1=NN=C2N1C=CC=C2)N

Technology Process of (R)-1-([1,2,4]triazolo[4,3-a]pyridin-3-yl)ethanamine

There total 6 articles about (R)-1-([1,2,4]triazolo[4,3-a]pyridin-3-yl)ethanamine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 915375-33-6
(1-[1,2,4]triazolo[4,3-a]pyridin-3-yl-ethyl)-carbamic acid tert-butyl ester

: 1217810-82-6,900641-16-9
1-[1,2,4]triazolo[4,3-a]pyridin-3-yl-ethylamine

Guidance literature:: With hydrogenchloride; In methanol;
DOI:10.1016/j.tetlet.2006.08.075

Reference yield:

: 915375-35-8
(1-[1,2,4]triazolo[4,3-a]pyridin-3-yl-ethyl)-carbamic acid tert-butyl ester

: 1217810-82-6,900641-16-9
1-[1,2,4]triazolo[4,3-a]pyridin-3-yl-ethylamine

Guidance literature:: With hydrogenchloride; In methanol;
DOI:10.1016/j.tetlet.2006.08.075

Reference yield:

: 915375-27-8
[1-(N'-pyridin-2-yl-hydrazinocarbonyl)-ethyl]-carbamic acid tert-butyl ester

: 1217810-82-6,900641-16-9
1-[1,2,4]triazolo[4,3-a]pyridin-3-yl-ethylamine

Guidance literature:: Multi-step reaction with 2 steps

1: 70 percent / Lawesson's reagent / 1,2-dimethoxy-ethane / 2 h / 80 °C

2: HCl / methanol

With Lawessons reagent; hydrogenchloride; In methanol; 1,2-dimethoxyethane;
DOI:10.1016/j.tetlet.2006.08.075