1-(3-Methoxyphenyl)piperazine

Suppliers

Names

[ CAS No. ]:
16015-71-7

[ Name ]:
1-(3-Methoxyphenyl)piperazine

[Synonym ]:
N-(3-methoxyphenyl)-piperazine
EINECS 240-154-8
Piperazine, 1-(3-methoxyphenyl)-
1-(3-methoxyphenyl)-piperazine
1-(m-methoxyphenyl)piperazine
3-methoxy-1-piperazinylbenzene
(3-methoxyphenyl)piperazine
MFCD00040733
3-(1-piperazinyl)anisole
4-(3-methoxyphenyl)piperazine
1-(3-Methoxyphenyl)piperazine

Chemical & Physical Properties

[ Density]:
1.1±0.1 g/cm3

[ Boiling Point ]:
344.0±27.0 °C at 760 mmHg

[ Melting Point ]:
201-204°C

[ Molecular Formula ]:
C11H16N2O

[ Molecular Weight ]:
192.258

[ Flash Point ]:
161.8±23.7 °C

[ Exact Mass ]:
192.126266

[ PSA ]:
24.50000

[ LogP ]:
1.01

[ Vapour Pressure ]:
0.0±0.8 mmHg at 25°C

[ Index of Refraction ]:
1.534

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS05

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H314

[ Precautionary Statements ]:
P280-P305 + P351 + P338-P310

[ Personal Protective Equipment ]:
Faceshields;full-face respirator (US);Gloves;Goggles;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
C:Corrosive;

[ Risk Phrases ]:
R34

[ Safety Phrases ]:
S26-S27-S36/37/39-S45

[ RIDADR ]:
UN 3267 8/PG 3

[ WGK Germany ]:
3

[ HS Code ]:
2933599090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • Piperazine
  • 3-Chloroanisole
  • Bis(2-Chloroethyl)amine hydrochloride
  • 3-anisidine
  • m-Bromoanisole
  • 3-Iodoanisole

DownStream

  • tert-butyl 4-(3-hydroxyphenyl)piperazine-1-carboxylate
  • 1-benzyl-4-(3-methoxyphenyl)piperazine
  • 3-(1-Piperazinyl)phenol
  • 1-(3-methoxyphenyl)-4-(2-pyridin-2-ylethyl)piperazine

Customs

[ HS Code ]: 2933599090

[ 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%

Articles

N-dealkylation of arylpiperazine derivatives: disposition and metabolism of the 1-aryl-piperazines formed. Caccia S.

Curr. Drug Metab. 8(6) , 612-22, (2007)


More Articles

Related Compounds

  • 1-(3-Methoxyphenyl)piperazine hydrochloride
  • 1-(3-Methoxyphenyl)piperazinedihydrochloride
  • 1-[(3-methoxyphenyl)-pyridin-4-ylmethyl]piperazine
  • 1-[(3-methoxyphenyl)methyl]-4-(naphthalen-1-ylmethyl)piperazine
  • 1-(3-methoxyphenyl)-4-[3-(4-nitrophenoxy)propyl]piperazine
  • 1-(3-methoxyphenyl)-4-(2-pyridin-2-ylethyl)piperazine
  • Methyl 2-chloro-8-fluoro-6-methylquinoline-3-carboxylate
  • 3-[4-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)hexanamido]oxolane-3-carboxylic acid
  • 6-Ethoxy-2-propoxyquinoline-3-carboxylic acid
  • 6-(2-Bromoethyl)-5-oxaspiro[3.4]octane
  • 4-(2,3-Difluorophenyl)-2,5-dimethylbenzaldehyde
  • N-[(4-tert-butyl-1,3-oxazol-2-yl)methyl]-2-chloropropanamide
  • N-[(4-tert-butyl-1,3-oxazol-2-yl)methyl]-2-chloroacetamide
  • 3-[(4-Nitrophenyl)methylidene]azetidine
  • 5-[(Azetidin-3-ylidene)methyl]-2-nitropyridine
  • 6-[(Azetidin-3-ylidene)methyl]-2-fluoropyridine-3-carbonitrile
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.