1,2-Dimethylindolizine

Base Information

• Chemical Name: 1,2-Dimethylindolizine
• CAS No.: 1125-77-5
• Molecular Formula: C₁₀H₁₁N
• Molecular Weight: 145.204
• Hs Code.: 2933990090
• DSSTox Substance ID: DTXSID40460068
• Nikkaji Number: J101.381E
• Wikidata: Q82283980
• Mol file: 1125-77-5.mol

Synonyms:1,2-dimethylindolizine;1125-77-5;dimethylindolizine;SCHEMBL7166909;DTXSID40460068

Chemical Property of 1,2-Dimethylindolizine

Chemical Property:

• PSA: 4.41000
• LogP: 2.55610
• XLogP3: 3.2
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 0
• Exact Mass: 145.089149355
• Heavy Atom Count: 11
• Complexity: 144

Purity/Quality:

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

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=CN2C=CC=CC2=C1C

Technology Process of 1,2-Dimethylindolizine

There total 9 articles about 1,2-Dimethylindolizine 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: 57.0%

2-(1-cyclopropylidene-ethyl)-pyridine → 1,2-dimethylindolizine (1125-77-5)

Guidance literature:

tetrakis(triphenylphosphine) palladium⁽⁰⁾; In acetonitrile; at 120 ℃; for 48h;

DOI:10.1021/jo050700s

Reference yield: 14.0%

2-Ethylpyridine (100-71-0) + chloroacetone (78-95-5) → 1,2-dimethylindolizine (1125-77-5)

Guidance literature:

at 130 ℃; for 24h; Inert atmosphere;

DOI:10.1002/chem.201702209

Reference yield:

2-Ethylpyridine (100-71-0) → 1,2-dimethylindolizine (1125-77-5)

Guidance literature:

With water; sodium hydrogencarbonate; chloroacetone;

DOI:10.1039/jr9530003654

upstream raw materials:

2-Ethylpyridine

1-(1,2-dimethyl-indolizin-3-yl)-ethanone

2-pyridyllithium

4-dimethylamino-3-methyl-2-[2]pyridyl-butan-2-ol

Downstream raw materials:

3-Aethyl-2-<4-(1,2-dimethyl-indolizin-(3)-yl)-butadien-(1,3)-yl>-benzthiazolium

(3-Bromo-4-hydroxy-phenyl)-(1,2-dimethyl-indolizin-3-yl)-methanone

[3-Bromo-4-(3-dibutylamino-propoxy)-phenyl]-(1,2-dimethyl-indolizin-3-yl)-methanone; compound with oxalic acid

bis(1,2-dimethyl-3-indolizinyl)methane

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