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Henan Allgreen Chemical Co.,LtdAmisulpride 71675-85-9//file1.lookchem.com/cas/reactions/2021/06/01/6876191.png

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Amisulpride 71675-85-9 CAS NO.71675-85-9

Min.Order Quantity:
1 Kilogram
Purity:
98%
Port:
shanghai
Payment Terms:
L/C,D/A,D/P,T/T,

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Product Details

Keywords

  • 71675-85-9
  • 71675-85-9
  • C17H27N3O4S

Quick Details

  • ProName: Amisulpride 71675-85-9
  • CasNo: 71675-85-9
  • Molecular Formula: C17H27N3O4S
  • Appearance: White or off-white Solid
  • DeliveryTime: 20day
  • PackAge: According to the demand of customer
  • Port: shanghai
  • ProductionCapacity: 20 Metric Ton/Month
  • Purity: 98%
  • Storage: Sealed, dry, microtherm , avoid light ...
  • Transportation: According to the demand of customer
  • LimitNum: 1 Kilogram

Superiority

amisulpride basic information
product name: amisulpride
synonyms: 4-amino-n-[(1-ethyl-2-pyrrolidinyl)methyl]-5-(ethylsulfonyl)-2-methoxybenzamide;amisulpride;aminosultopride;dan-2163;deniban;socian;solian;4-amino-n-((1-ethyl-2-pyrrolidinyl)methyl)-5-(ethylsulfonyl)-2-methoxybenzam
cas: 71675-85-9
mf: c17h27n3o4s
mw: 369.48
einecs: 275-831-7
product categories: active pharmaceutical ingredients;antipsychotic;drug analogues;intermediates & fine chemicals;pharmaceuticals;dopamine receptor;deniban
mol file: 71675-85-9.mol
amisulpride structure
amisulpride chemical properties
mp 124-128
storage temp. 2-8°c
solubility dmso: ≥5 mg/ml
form solid
color white
cas database reference 71675-85-9(cas database reference)
safety information
hazard codes xn
risk statements 22
safety statements 22-24/25
wgk germany 3
rtecs cv2308701
msds information
provider language
amisulpride english
sigmaaldrich english
amisulpride usage and synthesis
chemical properties off-white solid
usage neuroleptic agent, an analogue of sulpiride. used as an antipsychotic. dopamine receptor antagonist
usage amisulpride is a neuroleptic agent, an analogue of sulpiride (s689145). amisulpride is used as an antipsychotic. amisulpride is a dopamine receptor antagonist.
biological activity potent, selective dopamine d 2 and d 3 receptor antagonist. k i values are 2.8 and 3.2 nm respectively for human d 2 and d 3 and > 1000 nm for human d 1 , d 4 and d 5 receptors. shows selectivity for presynaptic dopamine autoreceptors at low doses and blocks postsynaptic d 2 /d 3 receptors at higher doses. preferentially interacts with limbic d 2 -like receptors in vivo . atypical antipsychotic/antischizophrenic agent with limited extrapyrimidal side effects and a profile distinct from that of haloperidol and remoxipride.

Details

amisulpride basic information
product name: amisulpride
synonyms: 4-amino-n-[(1-ethyl-2-pyrrolidinyl)methyl]-5-(ethylsulfonyl)-2-methoxybenzamide;amisulpride;aminosultopride;dan-2163;deniban;socian;solian;4-amino-n-((1-ethyl-2-pyrrolidinyl)methyl)-5-(ethylsulfonyl)-2-methoxybenzam
cas: 71675-85-9
mf: c17h27n3o4s
mw: 369.48
einecs: 275-831-7
product categories: active pharmaceutical ingredients;antipsychotic;drug analogues;intermediates & fine chemicals;pharmaceuticals;dopamine receptor;deniban
mol file: 71675-85-9.mol
amisulpride structure
amisulpride chemical properties
mp 124-128
storage temp. 2-8°c
solubility dmso: ≥5 mg/ml
form solid
color white
cas database reference 71675-85-9(cas database reference)
safety information
hazard codes xn
risk statements 22
safety statements 22-24/25
wgk germany 3
rtecs cv2308701
msds information
provider language
amisulpride english
sigmaaldrich english
amisulpride usage and synthesis
chemical properties off-white solid
usage neuroleptic agent, an analogue of sulpiride. used as an antipsychotic. dopamine receptor antagonist
usage amisulpride is a neuroleptic agent, an analogue of sulpiride (s689145). amisulpride is used as an antipsychotic. amisulpride is a dopamine receptor antagonist.
biological activity potent, selective dopamine d 2 and d 3 receptor antagonist. k i values are 2.8 and 3.2 nm respectively for human d 2 and d 3 and > 1000 nm for human d 1 , d 4 and d 5 receptors. shows selectivity for presynaptic dopamine autoreceptors at low doses and blocks postsynaptic d 2 /d 3 receptors at higher doses. preferentially interacts with limbic d 2 -like receptors in vivo . atypical antipsychotic/antischizophrenic agent with limited extrapyrimidal side effects and a profile distinct from that of haloperidol and remoxipride.

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