P-Dimethylaminobenzophenone anti-oxime

Base Information

Chemical Name:P-Dimethylaminobenzophenone anti-oxime
CAS No.:2998-95-0
Molecular Formula:C₁₅H₁₆N₂O
Molecular Weight:240.305
Hs Code.:
NSC Number:43963
UNII:354GIL0Y2V
Wikidata:Q27261273
ChEMBL ID:CHEMBL1975457

Synonyms:p-Dimethylaminobenzophenone syn-oxime;UNII-354GIL0Y2V;354GIL0Y2V;2998-95-0;p-Dimethylaminobenzophenone syn-oxime [MI];Benzophenone, 4-(dimethylamino)-, oxime, (Z)-;P-Dimethylaminobenzophenone anti-oxime;Methanone, (4-(dimethylamino)phenyl)phenyl-, oxime, (1Z)-;(NZ)-N-[[4-(dimethylamino)phenyl]-phenylmethylidene]hydroxylamine;NSC43963;6310-85-6;CHEMBL1975457;NSC-43963;SR-01000205365;SR-01000205365-1;Q27261273;Methanone, [4-(dimethylamino)phenyl]phenyl-, oxime, (Z)-

Suppliers and Price of P-Dimethylaminobenzophenone anti-oxime

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of P-Dimethylaminobenzophenone anti-oxime

Chemical Property:

XLogP3:3.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:240.126263138
Heavy Atom Count:18
Complexity:274

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CN(C)C1=CC=C(C=C1)C(=NO)C2=CC=CC=C2
Isomeric SMILES:CN(C)C1=CC=C(C=C1)/C(=N\O)/C2=CC=CC=C2

Technology Process of P-Dimethylaminobenzophenone anti-oxime

There total 5 articles about P-Dimethylaminobenzophenone anti-oxime 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:

: 28611-39-4
4-(dimethylamino)benzene-boronic acid

: 698-16-8
benzohydroximoyl chloride

: 2998-95-0
(4-(dimethylamino)phenyl)(phenyl)methanone oxime

: 2998-94-9
4-dimethylamino-benzophenone-seqtrans-oxime

Guidance literature:: With N,N-dimethyl-aniline; In chloroform; at 60 ℃; for 3h; Overall yield = 39 percent; Overall yield = 23.1 mg; Inert atmosphere;
DOI:10.1002/chem.202001590

Reference yield:

: 100-52-7
benzaldehyde

: 2998-95-0
(4-(dimethylamino)phenyl)(phenyl)methanone oxime

: 2998-94-9
4-dimethylamino-benzophenone-seqtrans-oxime

Guidance literature:: Multi-step reaction with 3 steps

1: sodium hydroxide; hydroxylamine hydrochloride / ethanol / 2 h / Reflux

2: N-chloro-succinimide / N,N-dimethyl-formamide / 6 h / 20 °C

3: N,N-dimethyl-aniline / chloroform / 3 h / 60 °C / Inert atmosphere

With N-chloro-succinimide; hydroxylamine hydrochloride; N,N-dimethyl-aniline; sodium hydroxide; In ethanol; chloroform; N,N-dimethyl-formamide;
DOI:10.1002/chem.202001590

Reference yield:

: 932-90-1
Benzaldoxime

: 2998-95-0
(4-(dimethylamino)phenyl)(phenyl)methanone oxime

: 2998-94-9
4-dimethylamino-benzophenone-seqtrans-oxime

Guidance literature:: Multi-step reaction with 2 steps

1: N-chloro-succinimide / N,N-dimethyl-formamide / 6 h / 20 °C

2: N,N-dimethyl-aniline / chloroform / 3 h / 60 °C / Inert atmosphere

With N-chloro-succinimide; N,N-dimethyl-aniline; In chloroform; N,N-dimethyl-formamide;
DOI:10.1002/chem.202001590