(R)-(-)-1-(alpha-AMINOBENZYL)-2-NAPHTHOL TARTARATE

Base Information

Chemical Name:(R)-(-)-1-(alpha-AMINOBENZYL)-2-NAPHTHOL TARTARATE
CAS No.:219897-36-6
Molecular Formula:C₄H₆O₆*C₁₇H₁₅NO
Molecular Weight:399.4
Hs Code.:
Mol file:219897-36-6.mol

Synonyms:(2R,3R)-2,3-dihydroxybutanedioic acid; 1-[(R)-amino(phenyl)methyl]naphthalen-2-ol;(R)-1-(Amino(phenyl)methyl)naphthalen-2-ol (2R,3R)-2,3-dihydroxysuccinate;(R)-(-)-1-(alpha-AMINOBENZYL)-2-NAPHTHOL TARTARATE

Suppliers and Price of (R)-(-)-1-(alpha-AMINOBENZYL)-2-NAPHTHOL TARTARATE

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
(R)-(-)-1-(ALPHA-AMINOBENZYL)-2-NAPHTHOL TARTRATE 95.00%
5MG
$ 503.39

Total 10 raw suppliers

Chemical Property of (R)-(-)-1-(alpha-AMINOBENZYL)-2-NAPHTHOL TARTARATE

Chemical Property:

PSA：161.31000
LogP:2.17120
Hydrogen Bond Donor Count:6
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:5
Exact Mass:399.13180201
Heavy Atom Count:29
Complexity:421

Purity/Quality:

99% ^*data from raw suppliers

(R)-(-)-1-(ALPHA-AMINOBENZYL)-2-NAPHTHOL TARTRATE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(C2=C(C=CC3=CC=CC=C32)O)N.C(C(C(=O)O)O)(C(=O)O)O
Isomeric SMILES:C1=CC=C(C=C1)[C@H](C2=C(C=CC3=CC=CC=C32)O)N.[C@@H]([C@H](C(=O)O)O)(C(=O)O)O

Technology Process of (R)-(-)-1-(alpha-AMINOBENZYL)-2-NAPHTHOL TARTARATE

There total 9 articles about (R)-(-)-1-(alpha-AMINOBENZYL)-2-NAPHTHOL TARTARATE 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: 98.0%