(r)-6-Bromo-2-aminotetralin

Base Information

Chemical Name:(r)-6-Bromo-2-aminotetralin
CAS No.:167172-92-1
Molecular Formula:C₁₀H₁₂BrN
Molecular Weight:226.116
Hs Code.:2921450090
DSSTox Substance ID:DTXSID30436035
Wikidata:Q82251216
Mol file:167172-92-1.mol

Synonyms:(r)-6-bromo-2-aminotetralin;167172-92-1;(2R)-6-Bromo-1,2,3,4-tetrahydronaphthalen-2-amine;(R)-6-Bromo-1,2,3,4-tetrahydronaphthalen-2-amine;2-Naphthalenamine, 6-bromo-1,2,3,4-tetrahydro-, (2R)-;SCHEMBL3020673;DTXSID30436035;WMALPFDUOAVVMB-SNVBAGLBSA-N

Suppliers and Price of (r)-6-Bromo-2-aminotetralin

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

American Custom Chemicals Corporation
(2R)-6-BROMO-2-1,2,3,4-TETRAHYDRONAPHTHYLAMINE 95.00%
5MG
$ 499.13

Total 4 raw suppliers

Chemical Property of (r)-6-Bromo-2-aminotetralin

Chemical Property:

Vapor Pressure:0.001mmHg at 25°C
Boiling Point:298.7 ºC at 760 mmHg
Flash Point:134.5ºC
PSA：26.02000
Density:1.413 g/cm³
LogP:2.96540
XLogP3:2.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:225.01531
Heavy Atom Count:12
Complexity:160

Purity/Quality:

99% ^*data from raw suppliers

(2R)-6-BROMO-2-1,2,3,4-TETRAHYDRONAPHTHYLAMINE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CC2=C(CC1N)C=CC(=C2)Br
Isomeric SMILES:C1CC2=C(C[C@@H]1N)C=CC(=C2)Br

Technology Process of (r)-6-Bromo-2-aminotetralin

There total 2 articles about (r)-6-Bromo-2-aminotetralin 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: 93.0%

: N-((R)-6-Bromo-1,2,3,4-tetrahydro-naphthalen-2-yl)-benzamide

: 167172-92-1,176707-78-1
2-Amino-6-bromo tetralin

Guidance literature:: With methanesulfonic acid; In acetic acid; at 160 ℃; for 24h;
DOI:10.1021/jo00119a008

Reference yield: 92.5%

: (R)-2-Azido-6-bromo-1,2,3,4-tetrahydro-naphthalene

: 167172-92-1,176707-78-1
2-Amino-6-bromo tetralin

Guidance literature:: With [2,2]bipyridinyl; sodium tetrahydroborate; cobalt(II) bromide; In ethanol; for 2h; Ambient temperature;
DOI:10.1021/jo00119a008