2-((4-Acetylphenyl)(nitroso)amino)acetic acid

Base Information

Chemical Name:2-((4-Acetylphenyl)(nitroso)amino)acetic acid
CAS No.:84968-84-3
Molecular Formula:C10H10N2O4
Molecular Weight:222.2
Hs Code.:
European Community (EC) Number:662-908-9

Synonyms:84968-84-3;2-((4-Acetylphenyl)(nitroso)amino)acetic acid;2-(4-acetyl-N-nitrosoanilino)acetic acid;2-[(4-acetylphenyl)(nitroso)amino]acetic acid;SCHEMBL2558482;AKOS024328263;SB80044;2-((4-Acetylphenyl)(nitroso)amino)aceticacid;EN300-134904;(1-(4-ACETYLPHENYL)-2-OXOHYDRAZINO)ACETIC ACID

Suppliers and Price of 2-((4-Acetylphenyl)(nitroso)amino)acetic acid

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

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Chemical Property of 2-((4-Acetylphenyl)(nitroso)amino)acetic acid

Chemical Property:

XLogP3:1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:4
Exact Mass:222.06405680
Heavy Atom Count:16
Complexity:285

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of 2-((4-Acetylphenyl)(nitroso)amino)acetic acid

There total 3 articles about 2-((4-Acetylphenyl)(nitroso)amino)acetic acid 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: 83.0%

: 42288-24-4
4-Carboxymethylamino-acetophenon

: 84968-84-3
N-nitroso-N-(4-acetylphenyl)glycine

Guidance literature:: With hydrogenchloride; sodium nitrite; In water; 1) 0-5 deg C, 30 min, 2) overnight;

Reference yield:

: 99-92-3
p-aminobenzophenone

: 84968-84-3
N-nitroso-N-(4-acetylphenyl)glycine

Guidance literature:: Multi-step reaction with 2 steps

1: 76 percent / H₂O / 40 h / Heating

2: 73 percent / aq. NaNO₂, 18percent HCl / methanol / 1 h / 0 - 5 °C

With hydrogenchloride; sodium nitrite; In methanol; water;
DOI:10.1002/ardp.19923250706

Reference yield:

: 99-92-3
p-aminobenzophenone

: 84968-84-3
N-nitroso-N-(4-acetylphenyl)glycine

Guidance literature:: Multi-step reaction with 2 steps

1: 88 percent / 2N sodium hydroxide / Heating

2: 83 percent / hydrochloric acid, sodium nitrite / H₂O / 1) 0-5 deg C, 30 min, 2) overnight

With hydrogenchloride; sodium hydroxide; sodium nitrite; In water;