4-(4-methylbenzyl)-1H-pyrazole-3,5-diamine

Base Information

Chemical Name:4-(4-methylbenzyl)-1H-pyrazole-3,5-diamine
CAS No.:109547-61-7
Molecular Formula:C₁₁H₁₄N₄
Molecular Weight:202.259
Hs Code.:
DSSTox Substance ID:DTXSID601228623

Synonyms:4-(4-methylbenzyl)-1H-pyrazole-3,5-diamine;109547-61-7;4-[(4-methylphenyl)methyl]-1H-pyrazole-3,5-diamine;1H-Pyrazole-3,5-diamine, 4-[(4-methylphenyl)methyl]-;DTXSID601228623;AKOS004903056;[5-amino-4-(p-tolyl-methyl)-2H-pyrazol-3-yl]-amine

Suppliers and Price of 4-(4-methylbenzyl)-1H-pyrazole-3,5-diamine

Supply Marketing:

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

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Total 1 raw suppliers

Chemical Property of 4-(4-methylbenzyl)-1H-pyrazole-3,5-diamine

Chemical Property:

XLogP3:1.8
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:202.121846464
Heavy Atom Count:15
Complexity:201

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=CC=C(C=C1)CC2=C(NN=C2N)N

Technology Process of 4-(4-methylbenzyl)-1H-pyrazole-3,5-diamine

There total 2 articles about 4-(4-methylbenzyl)-1H-pyrazole-3,5-diamine 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: 70.0%

: 5553-86-6
(4-methylbenzyl)malononitrile

: 109547-61-7
4-(4-Methyl-benzyl)-1H-pyrazole-3,5-diamine

Guidance literature:: With hydrazine hydrate; In ethanol; for 8h; Heating;
DOI:10.1055/s-1987-27831

Reference yield:

: 104-87-0
4-methyl-benzaldehyde

: 109547-61-7
4-(4-Methyl-benzyl)-1H-pyrazole-3,5-diamine

Guidance literature:: Multi-step reaction with 2 steps

1: sodium tetrahydroborate; hydrogenchloride / ethanol; water / 20 °C

2: hydrazine hydrate / ethanol / Reflux

With hydrogenchloride; sodium tetrahydroborate; hydrazine hydrate; In ethanol; water;
DOI:10.1016/j.ejmech.2014.03.063