(S)-1,2,3,4-tetrahydro-1-naphthylamine

Base Information Edit

Chemical Name:(S)-1,2,3,4-tetrahydro-1-naphthylamine
CAS No.:23357-52-0
Molecular Formula:C10H13N
Molecular Weight:147.22
Hs Code.:29214500
European Community (EC) Number:629-348-7
UNII:CB11LAU5CV
DSSTox Substance ID:DTXSID301335744
Nikkaji Number:J807.759B
Wikidata:Q27895862
ChEMBL ID:CHEMBL39537
Mol file:23357-52-0.mol

Synonyms:23357-52-0;(S)-1,2,3,4-tetrahydro-1-naphthylamine;(S)-1,2,3,4-Tetrahydronaphthalen-1-amine;(S)-(+)-1,2,3,4-Tetrahydro-1-naphthylamine;(1S)-1,2,3,4-tetrahydronaphthalen-1-amine;1-Aminotetralin, (S)-;(S)-(+)-1-Aminotetraline;1-NAPHTHALENAMINE, 1,2,3,4-TETRAHYDRO-, (1S)-;CB11LAU5CV;(S)-1-AMINOTETRALIN;CHEMBL39537;(1S)-(+)-1-Amino-1,2,3,4-tetrahydronaphthalene;MFCD00671630;(S)-1,2,3,4-tetrahydro-naphthalen-1-ylamine;(S)-1-Amino-1,2,3,4-tetrahydro-naphthalene;EC 629-348-7;(1~{S})-1,2,3,4-tetrahydronaphthalen-1-amine;(S)-1-AMINO-1,2,3,4-TETRAHYDRONAPHTHALENE;32908-38-6;1,2,3,4-Tetrahydro-naphthalen-1-ylamine;STQ;(s)-amino tetralin;S-1-Aminotetraline;Tetralin-1beta-amine;UNII-CB11LAU5CV;D0UF1R;SCHEMBL44600;(+)-1-AMINOTETRALIN;1-AMINOTETRALIN, (+)-;JRZGPXSSNPTNMA-JTQLQIEISA-N;DTXSID301335744;STR08071;BDBM50023876;AKOS006341644;CS-W008303;(S)-1,2,3,4-tetrahydronaphthaleneamine;AC-26799;(S)-1,2,3,4-tetrahydro-1-naphtylamine;(+)-1,2,3,4-Tetrahydro-1-naphthylamine;(1S)-1,2,3,4-tetrahydro-1-naphthylamine;AM20060563;T2878;(1S)-1,2,3,4-tetrahydro-1-naphthalenylamine;(S)-1,2,3,4-tetrahydro-naphthaien-1-ylamine;EN300-330138;(S)-(+)-1,2,3,4,-Tetrahydro-1-naphthylamine;(S)-(+)-1-Amino-1,2,3,4-tetrahydronaphthalene;A816685;J-015082;1-naphthalenamine, 1,2,3,4-tetrahydro-, (1s)- =;Q27895862;(1S)-1,2,3,4-TETRAHYDRO-.ALPHA.-NAPHTHYLAMINE;(S)-(+)-(1,2,3,4-Tetrahydro-naphthalen-1-yl)amine;(S)-(+)-1,2,3,4-Tetrahydro-1-naphthylamine, 97%;F8886-0006;(S)-(1,2,3,4-TETRAHYDRO-NAPHTHALEN-1-YL)AMINE;(S)-(+)-1,2,3,4-Tetrahydro-1-naphthylamine, ChiPros(R), produced by BASF, 99%

Suppliers and Price of (S)-1,2,3,4-tetrahydro-1-naphthylamine

Supply Marketing:Edit

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

TRC
S-(+)-1-Aminotetrahydronaphthalene
10g
$ 165.00

TCI Chemical
(S)-(+)-1,2,3,4-Tetrahydro-1-naphthylamine
25G
$ 231.00

TCI Chemical
(S)-(+)-1,2,3,4-Tetrahydro-1-naphthylamine
5G
$ 76.00

SynQuest Laboratories
(1S)-(+)-1-Amino-1,2,3,4-tetrahydronaphthalene
5 g
$ 37.00

SynQuest Laboratories
(1S)-(+)-1-Amino-1,2,3,4-tetrahydronaphthalene
1 g
$ 16.00

SynQuest Laboratories
(1S)-(+)-1-Amino-1,2,3,4-tetrahydronaphthalene
25 g
$ 106.00

Sigma-Aldrich
(S)-(+)-1,2,3,4-Tetrahydro-1-naphthylamine 97%
5g
$ 87.30

Sigma-Aldrich
(S)-(+)-1,2,3,4-Tetrahydro-1-naphthylamine ChiPros , produced by BASF, 99%
100g
$ 910.00

Sigma-Aldrich
(S)-(+)-1,2,3,4-Tetrahydro-1-naphthylamine ChiPros , produced by BASF, 99%
25g
$ 309.00

Sigma-Aldrich
(S)-(+)-1,2,3,4-Tetrahydro-1-naphthylamine 97%
25g
$ 309.00

Total 100 raw suppliers

Chemical Property of (S)-1,2,3,4-tetrahydro-1-naphthylamine Edit

Chemical Property:

Vapor Pressure:0.00205mmHg at 25°C
Refractive Index:1.565
Boiling Point:249.6 °C at 760 mmHg
PKA:9.39±0.20(Predicted)
Flash Point:110.8 °C
PSA：26.02000
Density:1.023 g/cm³
LogP:2.72300
Storage Temp.:Keep in dark place,Inert atmosphere,Room temperature
Sensitive.:Air Sensitive
Water Solubility.:Soluble in water.
XLogP3:1.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:147.104799419
Heavy Atom Count:11
Complexity:133

Purity/Quality:

99% ^*data from raw suppliers

S-(+)-1-Aminotetrahydronaphthalene ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xi; N, C
Hazard Codes:Xi,N,C
Statements: 36/37-51/53-36/37/38-34-52/53-22
Safety Statements: 26-36/37/39-61-45

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CC(C2=CC=CC=C2C1)N
Isomeric SMILES:C1C[C@@H](C2=CC=CC=C2C1)N
Uses A chiral amine derivative, (S)-1,2,3,4-Tetrahydro-1-naphthalenamine can be used in studies of real-time chiral discrimination of enantiomers as well as in studies of kinetic resolution of chiral amines with ω-transaminase using an enzyme-membrane re actor. (S)-(+)-1,2,3,4-Tetrahydro-1-naphthylamine is used as a chiral amine derivative used in studies of real-time chiral discrimination of enantiomers as well as in studies of kinetic resolution of chiral amines with ω-transaminase using an enzyme-membrane reactor.

Technology Process of (S)-1,2,3,4-tetrahydro-1-naphthylamine

There total 36 articles about (S)-1,2,3,4-tetrahydro-1-naphthylamine 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: 88.0%

: (S)-1,2,3,4-tetrahydronaphthalene-1-carbamic acid tert-butyl ester

: 23357-52-0
(S)-1,2,3,4-tetrahydronapht-1-yl-amine

Guidance literature:: With trifluorormethanesulfonic acid; In dichloromethane; at 20 ℃; for 2h; Schlenk technique; Inert atmosphere;
DOI:10.1021/acs.orglett.6b02300

Reference yield: 86.0%

: 104354-39-4,192461-77-1
3,4-dihydro-naphthalen-1(2H)-one oxime O-methyl ether

: 23357-52-0
(S)-1,2,3,4-tetrahydronapht-1-yl-amine

: 23357-46-2
(R)-1,2,3,4-Tetrahydro-1-naphthylamine

Guidance literature:: With sodium tetrahydroborate; (S)-valinol; zirconium(IV) chloride; In tetrahydrofuran; Title compound not separated from byproducts; Ambient temperature;