1-(4-tert-Butylbenzyl)piperazine - CAS 956-61-6
Catalog: |
BB041800 |
Product Name: |
1-(4-tert-Butylbenzyl)piperazine |
CAS: |
956-61-6 |
Synonyms: |
1-[(4-tert-butylphenyl)methyl]piperazine |
IUPAC Name: | 1-[(4-tert-butylphenyl)methyl]piperazine |
Description: | 1-(4-tert-Butylbenzyl)piperazine (CAS# 956-61-6) is a useful research chemical. |
Molecular Weight: | 232.36 |
Molecular Formula: | C15H24N2 |
Canonical SMILES: | CC(C)(C)C1=CC=C(C=C1)CN2CCNCC2 |
InChI: | InChI=1S/C15H24N2/c1-15(2,3)14-6-4-13(5-7-14)12-17-10-8-16-9-11-17/h4-7,16H,8-12H2,1-3H3 |
InChI Key: | UQLCETYSARZZSR-UHFFFAOYSA-N |
Boiling Point: | 138-140 °C / 2 mmHg |
Density: | 0.974 g/cm3 |
MDL: | MFCD00082594 |
LogP: | 2.65600 |
GHS Hazard Statement: | H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation] |
Precautionary Statement: | P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
CN-113214275-A | Pyranocarbazole alkaloid derivatives and their use for treating nervous system diseases | 20200204 |
US-2020399271-A1 | Xanthine analogs as potent anti-west nile viral agents | 20190620 |
CN-109666027-A | GPR40 agonist compound of a kind of amide structure and application thereof | 20171017 |
US-2021113534-A1 | Compounds | 20170517 |
US-2020262813-A1 | 1,5,7-trisubstituted isoquinoline derivatives, preparation thereof, and use thereof in medicines | 20161111 |
Complexity: | 218 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 232.193948774 |
Formal Charge: | 0 |
Heavy Atom Count: | 17 |
Hydrogen Bond Acceptor Count: | 2 |
Hydrogen Bond Donor Count: | 1 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 232.193948774 |
Rotatable Bond Count: | 3 |
Topological Polar Surface Area: | 15.3 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 2.8 |
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