(R)-5-Bromo-indan-2-ylamine

Base Information

Chemical Name:(R)-5-Bromo-indan-2-ylamine
CAS No.:321352-53-8
Molecular Formula:C9H10BrN
Molecular Weight:212.089
Hs Code.:
DSSTox Substance ID:DTXSID10460893
Wikidata:Q76416906
Mol file:321352-53-8.mol

Synonyms:321352-53-8;(R)-5-Bromo-indan-2-ylamine;1H-Inden-2-amine, 5-bromo-2,3-dihydro-, (2R)-;(R)-5-Bromo-2,3-dihydro-1H-inden-2-amine;(r)-5-bromo-2-aminoindan;(R)-5-bromo-indan-2-yl-amine;(R)-5-bromo-2-aminoindane;(R)-5-bromoindan-2-ylamine;SCHEMBL419456;(2R)-5-BROMO-2,3-DIHYDRO-1H-INDEN-2-AMINE;DTXSID10460893;RWAVYCTUVYJSMU-SECBINFHSA-N

Suppliers and Price of (R)-5-Bromo-indan-2-ylamine

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

Total 1 raw suppliers

Chemical Property of (R)-5-Bromo-indan-2-ylamine

Chemical Property:

XLogP3:2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:210.99966
Heavy Atom Count:11
Complexity:149

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1C(CC2=C1C=CC(=C2)Br)N
Isomeric SMILES:C1[C@H](CC2=C1C=CC(=C2)Br)N

Technology Process of (R)-5-Bromo-indan-2-ylamine

There total 1 articles about (R)-5-Bromo-indan-2-ylamine 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: 26.0%

: 35963-20-3,61380-66-3
(R)-10-camphorsulfonic acid

: 321352-52-7
5-bromo-2-aminoindane hydrobromide

: 321352-53-8
(R)-5-bromo-2,3-dihydro-1H-inden-2-amine

: 370861-57-7
(S)-5-bromo-2-aminoindan (1R)-(-)-10-camphorsulfonate salt

Guidance literature:: With 4-methylmorpholine N-oxide; In methanol; at 65 ℃; Resolution of racemate;
DOI:10.1016/j.bmcl.2010.11.098

Reference yield: 86.0%

: 459-60-9
1-fluoro-4-methoxybenzene

: 321352-53-8
(R)-5-bromo-2,3-dihydro-1H-inden-2-amine

: 5-bromo-N-(4-methoxyphenyl)-2,3-dihydro-1H-inden-2-amine

Guidance literature:: With 3,6‐di‐tert‐butyl‐9‐mesityl‐10‐phenylacridin‐10‐ium tetrafluoroborate; In 1,2-dichloro-ethane; at 20 ℃; for 72h; Inert atmosphere; Irradiation; Schlenk technique;
DOI:10.1002/chem.202002315

Reference yield:

: 630125-57-4
4-(4-ethylaminopyrimidin-6-yloxy)-aniline

: 321352-53-8
(R)-5-bromo-2,3-dihydro-1H-inden-2-amine

: N-(4-(4-ethylaminopyrimidin-6-yloxy)-phenyl)-N'-[(R)-5-bromo-indan-2-yl]urea

Guidance literature:: (R)-5-bromo-2,3-dihydro-1H-inden-2-amine; With bis(trichloromethyl) carbonate; triethylamine; In dichloromethane; at 0 - 20 ℃; for 1h;

4-(4-ethylaminopyrimidin-6-yloxy)-aniline; With triethylamine; In dichloromethane; at 20 ℃; for 16h;