2-iodo-N,N-dimethylacetamide

Base Information

• Chemical Name: 2-iodo-N,N-dimethylacetamide
• CAS No.: 73664-43-4
• Molecular Formula: C4H8INO
• Molecular Weight: 213.018
• Hs Code.: 2924199090
• European Community (EC) Number: 845-780-0
• DSSTox Substance ID: DTXSID20223895
• Nikkaji Number: J74.876E
• Wikidata: Q83102394
• Mol file: 73664-43-4.mol

Synonyms:2-iodo-N,N-dimethylacetamide;73664-43-4;N,N-Dimethyl-2-iodoacetamide;ACETAMIDE, N,N-DIMETHYL-2-IODO-;BRN 4952103;C4H8INO;Acetamide, 2-iodo-N,N-dimethyl-;2-iodo-N,N-dimethyl-acetamide;SCHEMBL1564895;C4-H8-I-N-O;DTXSID20223895;MFCD01670617;AKOS014114603;LS-9372;ACETAMIDE,N,N-DIMETHYL-2-IODO-;AM805909;AS-59520;CS-0239613;EN300-216063

Chemical Property of 2-iodo-N,N-dimethylacetamide

Chemical Property:

• Vapor Pressure: 0.127mmHg at 25°C
• Boiling Point: 218.2°Cat760mmHg
• PKA: -0.95±0.70(Predicted)
• Flash Point: 85.8°C
• PSA: 20.31000
• Density: 1.808g/cm³
• LogP: 0.50960
• XLogP3: 0.4
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 212.96506
• Heavy Atom Count: 7
• Complexity: 72.1

Purity/Quality:

99% ^*data from raw suppliers

2-iodo-N,N-dimethylacetamide ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CN(C)C(=O)CI

Technology Process of 2-iodo-N,N-dimethylacetamide

There total 1 articles about 2-iodo-N,N-dimethylacetamide 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: 53.0%

2-chloro-N,N-dimethylacetamide (2675-89-0) → 2-iodo-N,N-dimethylacetamide (73664-43-4)

Guidance literature:

With sodium iodide; In acetonitrile; at 60 ℃; for 2h;

Reference yield: 90.0%

6,7-dimethoxy-2-methyl-1-phenyl-1,2,3,4-tetrahydroisoquinoline (4008-69-9,136904-97-7) + 2-iodo-N,N-dimethylacetamide (73664-43-4) → (+/-)-trans-6,7-dimethoxy-N-[(N',N'-dimethylcarbamoyl)methyl]-N-methyl-1-phenyl-1,2,3,4-tetrahydroisoquinolinium iodide

Guidance literature:

In acetone; at 20 ℃; for 24h; Inert atmosphere;

DOI:10.1002/ejoc.201000512

Reference yield: 65.0%

1-Decene (872-05-9,17438-89-0,25189-70-2) + 2-iodo-N,N-dimethylacetamide (73664-43-4) → gamma-dodecalactone (57084-18-1,2305-05-7)

Guidance literature:

With bis(tri-n-butyltin); ethyl iodide; Irradiation;

DOI:10.1021/ja00230a044

upstream raw materials:

2-chloro-N,N-dimethylacetamide

Downstream raw materials:

gamma-dodecalactone

N-[7-(dimethylcarbamoylmethyl-methyl-amino)-4-methoxy-benzothiazol-2-yl]-4-fluoro-benzamide

N-[7-(dimethylcarbamoylmethyl-ethyl-amino)-4-methoxy-benzothiazol-2-yl]-4-fluoro-benzamide

4-Nitrobenzyl (1S,5R,6S)-2-[6-(N,N-dimethyl-carbamoylmethyl)-7-methylthioimidazo[5,1-b]thiazolium-2-yl]-6-((1R)-1-hydroxyethyl)-1-methyl-1-carbapen-2-em3-carboxylate iodide

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