Imidafenacin metabolite M10

Base Information

Chemical Name:Imidafenacin metabolite M10
CAS No.:503598-33-2
Molecular Formula:C₁₈H₂₁N₃O
Molecular Weight:295.384
Hs Code.:
UNII:6C8P8BU7WV
Nikkaji Number:J2.473.322J
Mol file:503598-33-2.mol

Synonyms:503598-33-2;Imidafenacin metabolite M10;UNII-6C8P8BU7WV;6C8P8BU7WV;4-((Acetimidoyl)amino)-2,2-diphenylbutanamide;IMidafenacin Related CoMpound 6 (4-AcetiMidoylaMino-2,2-DiphenylbutanaMide);4-(1-aminoethylideneamino)-2,2-diphenylbutanamide;alpha-(2-((1-Iminoethyl)amino)ethyl)-alpha-phenylbenzeneacetamide;Benzeneacetamide, alpha-(2-((1-iminoethyl)amino)ethyl)-alpha-phenyl-;4-Acetimidoylamino-2,2-Diphenylbutanamide;.ALPHA.-(2-((1-IMINOETHYL)AMINO)ETHYL)-.ALPHA.-PHENYLBENZENEACETAMIDE;BENZENEACETAMIDE, .ALPHA.-(2-((1-IMINOETHYL)AMINO)ETHYL)-.ALPHA.-PHENYL-

Suppliers and Price of Imidafenacin metabolite M10

Supply Marketing:

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

Total 7 raw suppliers

Chemical Property of Imidafenacin metabolite M10

Chemical Property:

XLogP3:1.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:6
Exact Mass:295.168462302
Heavy Atom Count:22
Complexity:375

Purity/Quality:: > 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(=NCCC(C1=CC=CC=C1)(C2=CC=CC=C2)C(=O)N)N

Technology Process of Imidafenacin metabolite M10

There total 4 articles about Imidafenacin metabolite M10 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: 61.0%

: 503598-78-5
4-amino-2-diphenylbutanamide

: 41795-82-8
S-benzyl thioacetimidate hydrobromide

: 503598-33-2
4-[(acetimidoyl)amino]-2,2-diphenylbutanamide

Guidance literature:: In ethanol; at 0 ℃; for 2h;
DOI:10.1248/cpb.55.1039

Reference yield:

: 503598-74-1
C₃₀H₃₀N₂O

: 503598-33-2
4-[(acetimidoyl)amino]-2,2-diphenylbutanamide

Guidance literature:: Multi-step reaction with 2 steps

1: H₂ / Perlman's catalyst

2: 61 percent / ethanol / 2 h / 0 °C

With hydrogen; palladium hydroxide - carbon; In ethanol;
DOI:10.1248/cpb.55.1039

Reference yield:

: 86-29-3
Diphenylacetonitrile

: 503598-33-2
4-[(acetimidoyl)amino]-2,2-diphenylbutanamide

Guidance literature:: Multi-step reaction with 4 steps

1: NaH / dimethylformamide

2: aq. KOH / propan-2-ol

3: H₂ / Perlman's catalyst

4: 61 percent / ethanol / 2 h / 0 °C

With potassium hydroxide; hydrogen; sodium hydride; palladium hydroxide - carbon; In ethanol; N,N-dimethyl-formamide; isopropyl alcohol;
DOI:10.1248/cpb.55.1039