1,1,2-Trimethyl-1H-benzo[E]indole

Base Information Edit

Chemical Name:1,1,2-Trimethyl-1H-benzo[E]indole
CAS No.:41532-84-7
Deprecated CAS:1924617-96-8
Molecular Formula:C15H15N
Molecular Weight:209.291
Hs Code.:29339900
European Community (EC) Number:255-429-8
UNII:F56431T911
DSSTox Substance ID:DTXSID4044668
Nikkaji Number:J28.051H
Wikidata:Q27277660
ChEMBL ID:CHEMBL1405775
Mol file:41532-84-7.mol

Synonyms:41532-84-7;1,1,2-TRIMETHYL-1H-BENZO[E]INDOLE;1,1,2-Trimethylbenz[e]indole;1,1,2-TRIMETHYL-1H-BENZ[E]INDOLE;2,3,3-trimethylbenzoindolenine;2,3,3-Trimethyl-4,5-benzo-3H-indole;1,1,2-trimethylbenzo[e]indole;1H-BENZ[E]INDOLE, 1,1,2-TRIMETHYL-;1,1,2-Trimethyl-1H-benz(e)indole;MFCD00082627;1H-Benz(e)indole, 1,1,2-trimethyl-;DTXSID4044668;UNII-F56431T911;EINECS 255-429-8;1,1-2-Trimethyl-1H-benz(e)indole;F56431T911;1,1,2-trimethyl-1h-benzo(e)indole;1,1,2-TRIMETHYLBENZ(E)INDOLE;2,3,3-Trimethylbenzo[e]indolenine;1,1,2-Trimehtyl-1H-benz[e]indole;2,3,3-trimethyl-1H-benz[e]indolenine;SCHEMBL31583;MLS001018037;CHEMBL1405775;DTXCID2024668;HMS2663B13;Tox21_301959;CCG-53010;1,1,2-trimethyl[1H]-benz[e]indole;AKOS000270783;AKOS025243391;AM85760;CS-W015153;PS-8025;1,1,2-trimethyl-[1H]-benz[e]indole;2,3,3-Trimethylnaphto[1,2-d]pyrrole;1,1,2-Trimethylnaphtho[1,2-d]pyrrole;NCGC00245998-01;NCGC00256303-01;AC-27784;SMR000354277;SY018592;2,3,3-TRIMETHYL-3H-BENZ(E)INDOLE;CAS-41532-84-7;EU-0010594;FT-0601282;T1714;EN300-16734;H11740;T-6620;A825585;SR-01000389684;1,1,2-Trimethylbenz[e]indole, >=98.0% (HPLC);Q-102567;SR-01000389684-1;SR-01000389684-2;BRD-K67859649-001-07-6;Q27277660;Z56758999;F0347-1365

Suppliers and Price of 1,1,2-Trimethyl-1H-benzo[E]indole

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
1,1,2-Trimethyl-1H-benzo[e]indole
10g
$ 85.00

TCI Chemical
1,1,2-Trimethyl-1H-benzo[e]indole >98.0%(HPLC)(T)
100g
$ 157.00

TCI Chemical
1,1,2-Trimethyl-1H-benzo[e]indole >98.0%(HPLC)(T)
25g
$ 40.00

TCI Chemical
1,1,2-Trimethyl-1H-benzo[e]indole >98.0%(HPLC)(T)
5g
$ 13.00

SynQuest Laboratories
1,1,2-Trimethyl-1H-benzo[e]indole 99%
5 g
$ 20.00

SynQuest Laboratories
1,1,2-Trimethyl-1H-benzo[e]indole 99%
25 g
$ 31.00

SynQuest Laboratories
1,1,2-Trimethyl-1H-benzo[e]indole 99%
100 g
$ 93.00

Sigma-Aldrich
1,1,2-Trimethylbenz[e]indole ≥98.0% (HPLC)
25g-f
$ 84.50

Sigma-Aldrich
1,1,2-Trimethylbenz[e]indole ≥98.0% (HPLC)
25 g
$ 86.60

Matrix Scientific
1,1,2-Trimethyl-1H-benzo[e]indole 95%+
5g
$ 323.00

Total 133 raw suppliers

Chemical Property of 1,1,2-Trimethyl-1H-benzo[E]indole Edit

Chemical Property:

Appearance/Colour:yellow to brown crystalline powder
Vapor Pressure:0.00026mmHg at 25°C
Melting Point:111-117 °C
Refractive Index:1.6
Boiling Point:333.7 °C at 760 mmHg
PKA:5.77±0.40(Predicted)
Flash Point:147.7 °C
PSA：12.36000
Density:1.06 g/cm³
LogP:3.65900
Storage Temp.:Inert atmosphere,Room Temperature
Solubility.:insoluble (20°C)
Water Solubility.:insoluble (20 ºC)
XLogP3:3.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:209.120449483
Heavy Atom Count:16
Complexity:315

Purity/Quality:

99% ^*data from raw suppliers

1,1,2-Trimethyl-1H-benzo[e]indole ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xi, T
Hazard Codes:Xi,T
Statements: 36/37/38-45
Safety Statements: 26-36-53-45-37/39

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=NC2=C(C1(C)C)C3=CC=CC=C3C=C2
Uses 1,1,2-Trimethyl-1H-benzo[e]indole can be used as an indole pH fluorescent probe and can be used for intracellular pH detection and cell marking. It can also be used as a novel nanocarrier-based near-infrared optical probes for in-vivo tumor imaging.

Technology Process of 1,1,2-Trimethyl-1H-benzo[E]indole

There total 6 articles about 1,1,2-Trimethyl-1H-benzo[E]indole 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: 95.0%