Cas no 95356-15-3 (1-(o-Tolyl)piperazine hydrochloride)

1-(o-Tolyl)piperazine hydrochloride is a versatile organic compound known for its potent chemical properties. This compound offers excellent solubility in water and organic solvents, making it suitable for various chemical reactions. Its piperazine backbone provides flexibility for functional group substitution, enhancing its potential applications in organic synthesis. The hydrochloride salt form is stable and easy to handle, ensuring consistent performance in laboratory settings.
1-(o-Tolyl)piperazine hydrochloride structure
95356-15-3 structure
Product Name:1-(o-Tolyl)piperazine hydrochloride
CAS No:95356-15-3
MF:C11H17ClN2
MW:212.719081640244
MDL:MFCD00039030
CID:751868
PubChem ID:87576970
Update Time:2025-10-16

1-(o-Tolyl)piperazine hydrochloride Chemical and Physical Properties

Names and Identifiers

    • 1-(o-Tolyl)piperazine hydrochloride
    • 1-o-tolylpiperazine hydrochloride
    • Piperazine, 1-(2-methylphenyl)-, monohydrochloride
    • ortho-tolylpiperazine hydrochloride
    • 1-(2-Methylphenyl)piperazine Hydrochloride
    • N-(2-Methylphenyl)piperazine hydrochloride
    • 1-(2-Tolyl)piperazine hydrochloride
    • Piperazine, 1-(2-methylphenyl)-, hydrochloride
    • 1-(O-Tolyl)piperazine, HCl
    • PIP060
    • LZNYIWJDVYCKDU-UHFFFAOYSA-N
    • 1-o-tolyl-piperazine hydrochloride
    • NSC28784
    • N-(o-Tolyl)piperazine hydrochlorid
    • Piperazine, 1-(2-methylphenyl)-, monohydrochloride (9CI)
    • 1-(2-methylphenyl)piperazine hydrochloride (1:1)
    • 1-(2-Methylphenyl)piperazine monohydrochloride
    • 1-o-Tolylpiperazine monohydrochloride
    • 4-o-Tolylpiperazine monohydrochloride
    • SR-01000632350-1
    • 1-(o-tolyl) piperazine hydrochloride
    • 70849-60-4
    • AKOS009031233
    • AC-8983
    • MFCD00039030
    • SCHEMBL615080
    • 95356-15-3
    • VDA35615
    • SY014770
    • F21265
    • J-503048
    • 1-(o-Tolyl)piperazine hydrochloride, 97%
    • T1187
    • 1-(ortho-tolyl)piperazine hydrochloride
    • NSC-28784
    • 1-(2-methylphenyl)piperazine;hydrochloride
    • ortho-methylphenylpiperazine hydrochloride
    • DB-018470
    • N-(o-Tolyl)piperazine hydrochloride
    • MDL: MFCD00039030
    • Inchi: 1S/C11H16N2.ClH/c1-10-4-2-3-5-11(10)13-8-6-12-7-9-13;/h2-5,12H,6-9H2,1H3;1H
    • InChI Key: LZNYIWJDVYCKDU-UHFFFAOYSA-N
    • SMILES: Cl.C1C=C(N2CCNCC2)C(C)=CC=1

Computed Properties

  • Exact Mass: 212.10800
  • Monoisotopic Mass: 212.1080262g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 1
  • Complexity: 152
  • Covalently-Bonded Unit Count: 2
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 15.3

Experimental Properties

  • Melting Point: 240 °C
  • PSA: 15.27000
  • LogP: 2.60040

1-(o-Tolyl)piperazine hydrochloride Security Information

1-(o-Tolyl)piperazine hydrochloride Customs Data

  • HS CODE:2933599090
  • Customs Data:

    China Customs Code:

    2933599090

    Overview:

    2933599090. Other compounds with pyrimidine ring in structure(Including other compounds with piperazine ring on the structure. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%

    Declaration elements:

    Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date

    Summary:

    2933599090. other compounds containing a pyrimidine ring (whether or not hydrogenated) or piperazine ring in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

1-(o-Tolyl)piperazine hydrochloride Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
TRC
T536570-50mg
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$ 50.00 2022-03-29
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$ 50.00 2022-06-02
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1-(o-Tolyl)piperazine hydrochloride Production Method

Production Method 1

Reaction Conditions
1.1 Solvents: 1-Butanol ;  20 h, 130 °C
1.2 Reagents: Sodium bicarbonate ;  30 h, 130 °C
Reference
Synthesis of monoalkyl substituted phenylpiperazine derivatives
Bai, Baoqing; Yuan, Mu; Zhou, Xin, Jingxi Huagong, 2007, 24(8), 823-825

Production Method 2

Reaction Conditions
1.1 Solvents: 1-Butanol ;  rt; 24 h, reflux
1.2 Reagents: Potassium carbonate ;  48 h, reflux
Reference
Design, synthesis, and biological evaluation of structurally constrained hybrid analogues containing ropinirole moiety as a novel class of potent and selective dopamine D3 receptor ligands
Zhou, Benhua; Hong, Kwon Ho; Ji, Min; Cai, Jin, Chemical Biology & Drug Design, 2018, 92(3), 1597-1609

Production Method 3

Reaction Conditions
1.1 Solvents: Diethylene glycol monomethyl ether ;  4 min
Reference
Synthesis of N-aryl piperazinium chlorides under microwave irradiation
Fu, Li-xiang; Xu, Chong-fu; Lu, Hai-ling; Zheng, Huang-li; Zhao, Meng-meng; et al, Jingxi Huagong, 2013, 30(7), 816-820

Production Method 4

Reaction Conditions
1.1 Solvents: tert-Butanol ;  rt; 24 h, reflux
1.2 Reagents: Potassium carbonate ;  48 h, reflux
Reference
Design, synthesis and biological evaluation of bitopic arylpiperazine-hexahydro-pyrazinoquinolines as preferential dopamine D3 receptor ligands
Zhou, Benhua; Ji, Min; Cai, Jin, Bioorganic Chemistry, 2018, 77, 125-135

Production Method 5

Reaction Conditions
1.1 Solvents: 1-Butanol ;  24 h, 115 °C
1.2 Reagents: Sodium carbonate ;  22 h, 115 °C
Reference
Study on synthesis of 2-piperazinyl-4-phenylpyrimidine derivatives
Meng, Qi; Jiang, Nan; Jiang, Yan; Zhou, Changqing; Sun, Xiaoqiang, Huaxue Tongbao, 2013, 76(7), 624-629

Production Method 6

Reaction Conditions
Reference
Preparation of dihydroindol-2-one as the D3 receptor ligand
, China, , ,

Production Method 7

Reaction Conditions
Reference
Hexahydro-pyrazino quinolines D3 acceptor ligand, preparation method and application thereof
, China, , ,

1-(o-Tolyl)piperazine hydrochloride Raw materials

1-(o-Tolyl)piperazine hydrochloride Preparation Products

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