2,3-dihydro-1H-inden-4-amine

Base Information

• Chemical Name: 2,3-dihydro-1H-inden-4-amine
• CAS No.: 32202-61-2
• Molecular Formula: C9H11N
• Molecular Weight: 133.193
• Hs Code.: 2921499090
• European Community (EC) Number: 250-950-7
• NSC Number: 76664
• UNII: 3XLG4R478F
• DSSTox Substance ID: DTXSID30185975
• Nikkaji Number: J88.785D
• Wikidata: Q72438209
• Mol file: 32202-61-2.mol

Synonyms:2,3-dihydro-1H-inden-4-amine;32202-61-2;4-Aminoindan;4-Aminoindane;Indan-4-amine;1H-Inden-4-amine, 2,3-dihydro-;4-Indanamine;3XLG4R478F;EINECS 250-950-7;MFCD00082598;NSC-76664;indan-4-ylamine;4-amino-indane;4-amino-indan;indan-4-yl-amine;NSC76664;4-Aminoindan, 97%;UNII-3XLG4R478F;SCHEMBL353635;AMY6074;DTXSID30185975;NSC 76664;AKOS006220971;SB75402;DS-15208;SY106803;CS-0069588;FT-0731629;AE-646/31213054;W-202323

Chemical Property of 2,3-dihydro-1H-inden-4-amine

Chemical Property:

• Vapor Pressure: 0.0116mmHg at 25°C
• Melting Point: 9℃
• Refractive Index: n20/D 1.592(lit.)
• Boiling Point: 261.3 °C at 760 mmHg
• PKA: 4.49±0.20(Predicted)
• Flash Point: 123.5 °C
• PSA: 26.02000
• Density: 1.102 g/cm³
• LogP: 2.33870
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• XLogP3: 2.1
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 133.089149355
• Heavy Atom Count: 10
• Complexity: 122

Purity/Quality:

98%,99%, ^*data from raw suppliers

4-Aminoindan ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: C1CC2=C(C1)C(=CC=C2)N
• Uses: 4-Aminoindan was used in the synthesis of 4,5-dihydro-N-(2,3-dihydro-1H-inden-4-yl)oxazol-2-amine and 1-(2-chloroethyl)-3-(2,3-dihydro-1H-inden-4-yl)urea.

Technology Process of 2,3-dihydro-1H-inden-4-amine

There total 22 articles about 2,3-dihydro-1H-inden-4-amine 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: 91.0%

7-aminoindene → 4-aminoindan (32202-61-2)

Guidance literature:

With palladium on activated charcoal; hydrogen; In methanol; at 20 ℃;

Reference yield: 86.0%

4-nitroindane (34701-14-9) → 4-aminoindan (32202-61-2)

Guidance literature:

With hydrogen; palladium 10% on activated carbon; In ethanol; for 1h; under 2585.81 Torr;

Reference yield:

INDANE (496-11-7) → 4-aminoindan (32202-61-2)

Guidance literature:

Multistep reaction; (i) (nitration), (ii) H₂, Pd-C;

upstream raw materials:

INDANE

2,3-dihydro-1H-indene-4-carboxylic acid

4-nitroindane

Indanazolin-monohydrochlorid

Downstream raw materials:

4-indanol

indan-4-yl-dimethyl-amine

N-(1-Acetyl-2-imidazolin-2-yl)-N-(4-indanyl)amin

(+/-)-N-[7-(1-butyryl-pyrrolidin-3-ylsulfamoyl)-indan-4-yl]-2-methyl-benzamide