4-Methyl-alpha-(methylnitrosoamino)benzenemethanol acetate (ester)

Base Information

Chemical Name:4-Methyl-alpha-(methylnitrosoamino)benzenemethanol acetate (ester)
CAS No.:87096-68-2
Molecular Formula:C₁₁H₁₄N₂O₃
Molecular Weight:222.244
Hs Code.:
DSSTox Substance ID:DTXSID701007335

Synonyms:87096-68-2;4-Methyl-alpha-(methylnitrosoamino)benzenemethanol acetate (ester);DTXSID701007335;Benzenemethanol, 4-methyl-alpha-(methylnitrosoamino)-, acetate (ester);[Methyl(nitroso)amino](4-methylphenyl)methyl acetate

Suppliers and Price of 4-Methyl-alpha-(methylnitrosoamino)benzenemethanol acetate (ester)

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of 4-Methyl-alpha-(methylnitrosoamino)benzenemethanol acetate (ester)

Chemical Property:

XLogP3:2.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:4
Exact Mass:222.10044231
Heavy Atom Count:16
Complexity:250

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC=C(C=C1)C(N(C)N=O)OC(=O)C

Technology Process of 4-Methyl-alpha-(methylnitrosoamino)benzenemethanol acetate (ester)

There total 1 articles about 4-Methyl-alpha-(methylnitrosoamino)benzenemethanol acetate (ester) 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:

: 17972-13-3,29086-13-3,53699-34-6
p-methylbenzylidene-methylamine

: 563-63-3
silver(I) acetate

: 87096-68-2
N-<(α-Acetoxy)(4-methylphenyl)methyl>-N-nitrosomethylamin

Guidance literature:: With nitrosylchloride; Yield given. Multistep reaction. Yields of byproduct given. Title compound not separated from byproducts; 1.) CH₂Cl₂, 15 min, -30 deg C, 2.) from -20 deg C to room temp.; 12 h, room temp.;