N-Methyl-N-[(1-methyl-1H-imidazol-5-yl)methyl]amine

Base Information

• Chemical Name: N-Methyl-N-[(1-methyl-1H-imidazol-5-yl)methyl]amine
• CAS No.: 384821-19-6
• Molecular Formula: C6H11N3
• Molecular Weight: 125.173
• Hs Code.: 2933290090
• European Community (EC) Number: 867-570-8
• DSSTox Substance ID: DTXSID10428170
• Nikkaji Number: J1.688.140F
• Wikidata: Q82240968
• Mol file: 384821-19-6.mol

Synonyms:384821-19-6;N-Methyl-N-[(1-methyl-1H-imidazol-5-yl)methyl]amine;N-methyl-1-(3-methylimidazol-4-yl)methanamine;N-METHYL-1-(1-METHYL-1H-IMIDAZOL-5-YL)METHANAMINE;Methyl-(3-methyl-3H-imidazol-4-ylmethyl)-amine;1-Methyl-5-[(methylamino)methyl]-1H-imidazole;METHYL[(1-METHYL-1H-IMIDAZOL-5-YL)METHYL]AMINE;SCHEMBL46652;DTXSID10428170;YZCXLAHTHBVYGB-UHFFFAOYSA-N;MFCD07772801;AKOS006346198;AB42250;AS-6469;AT15467;N,3-Dimethyl-3H-imidazole-4-methanamine;CS-0308581;FT-0767668;EN300-1248288;J-523709;N-Methyl-n-[(1-methyl-1h-mdazol-5-yl)methyl]amne

Chemical Property of N-Methyl-N-[(1-methyl-1H-imidazol-5-yl)methyl]amine

Chemical Property:

• Vapor Pressure: 0.0119mmHg at 25°C
• Refractive Index: 1.54
• Boiling Point: 261 °C at 760 mmHg
• Flash Point: 111.6 °C
• PSA: 29.85000
• Density: 1.05 g/cm³
• LogP: 0.53040
• XLogP3: -0.6
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 125.095297364
• Heavy Atom Count: 9
• Complexity: 84.4

Purity/Quality:

98%min ^*data from raw suppliers

N-methyl-N-[(1-methyl-1H-imidazol-5-yl)methyl]amine ^*data from reagent suppliers

Safty Information:

• Pictogram(s): C
• Hazard Codes: C
• Statements: 34
• Safety Statements: 26-36/37/39

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CNCC1=CN=CN1C

Technology Process of N-Methyl-N-[(1-methyl-1H-imidazol-5-yl)methyl]amine

There total 4 articles about N-Methyl-N-[(1-methyl-1H-imidazol-5-yl)methyl]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:

Methyl-[1-(3-methyl-3H-imidazol-4-yl)-meth-(E)-ylidene]-amine → N-methyl-5-aminomethyl-1-methyl-1H-imidazole (384821-19-6)

Guidance literature:

With sodium tetrahydroborate; In methanol; water;

DOI:10.1021/jo010737m

Reference yield:

1-methylimidazole-5-carbaldehyde (39021-62-0) → N-methyl-5-aminomethyl-1-methyl-1H-imidazole (384821-19-6)

Guidance literature:

Multi-step reaction with 2 steps

1: methanol; H₂O / 20 °C

2: 16.3 g / NaBH₄ / methanol; H₂O

With sodium tetrahydroborate; In methanol; water;

DOI:10.1021/jo010737m

Reference yield:

(1-methyl-1H-imidazol-5-yl)methanol (38993-84-9) → N-methyl-5-aminomethyl-1-methyl-1H-imidazole (384821-19-6)

Guidance literature:

Multi-step reaction with 3 steps

1: 71 percent / MnO₂ / CHCl₃ / 48 h / Heating

2: methanol; H₂O / 20 °C

3: 16.3 g / NaBH₄ / methanol; H₂O

With manganese(IV) oxide; sodium tetrahydroborate; In methanol; chloroform; water;

DOI:10.1021/jo010737m

upstream raw materials:

1-methylimidazole-5-carbaldehyde

(1-methyl-1H-imidazol-5-yl)methanol

5-hydroxymethyl-2-mercapto-1-methyl-1H-imidazole

Downstream raw materials:

bis(5-methylaminomethyl-1-methyl-1H-2-imidazolyl)[1'-(2'-methoxyphenyl)-1'H-2'-imidazolyl]methyl methyl ether

bis(N-allyl-N-methyl-5'-aminomethyl-1'-methyl-1'H-2'-imidazolyl)[1''-(2''-methoxyphenyl)-1'H-2'-imidazolyl]methyl methyl ether

bis(N-allyl-N-methyl-5'-aminomethyl-1'-methyl-1'H-2'-imidazolyl)[1''-(2''-methoxyphenyl)-1'H-2'-imidazolyl]methyl alcohol

3-{3-[(2,2,2-trifluoro-ethyl)-ureido]-imidazo[1,2-a]pyridine-7-[5-(1-N-methyl-imidazole)]}-methylamide

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