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Merck
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重要文件

421235

Sigma-Aldrich

1-(2-嘧啶基)哌嗪

98%

同義詞:

2-(1-哌嗪基)嘧啶

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About This Item

經驗公式(希爾表示法):
C8H12N4
分子量::
164.21
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22
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化驗

98%

折射率

n20/D 1.587 (lit.)

bp

277 °C (lit.)

密度

1.158 g/mL at 25 °C (lit.)

SMILES 字串

C1CN(CCN1)c2ncccn2

InChI

1S/C8H12N4/c1-2-10-8(11-3-1)12-6-4-9-5-7-12/h1-3,9H,4-7H2

InChI 密鑰

MRBFGEHILMYPTF-UHFFFAOYSA-N

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一般說明

1-(2-嘧啶基)哌嗪是一种基于哌嗪的衍生物。[1]它是丁螺环酮的代谢产物。[2]

應用

1-(2-嘧啶基)哌嗪可用于以下研究:
  • 作为多肽羧基的衍生试剂。[1]
  • 磷酸肽分光光度分析过程中的羧基衍生化。[3]
  • 用于合成 3-{{(4-(嘧啶-2-基)哌嗪-1-基)甲基 }-1 H -吡咯并 [2,3- b ] 吡啶的起始试剂。[4]
  • 3-苯基-6-(4-(嘧啶-2-基)哌嗪-1-基)哒嗪-4-醇的合成。[5]

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

>230.0 °F

閃點(°C)

> 110 °C

個人防護裝備

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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B J Cao et al.
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It has been suggested that in vivo formation of the metabolite 1-(2-pyrimidinyl)-piperazine (1-PP) may be a major drawback in the use of buspirone as an anti-anxiety agent. To test this hypothesis, the effects of buspirone, alone or with proadifen (an
I Berlin et al.
British journal of clinical pharmacology, 39(3), 243-249 (1995-03-01)
1. Because the 5-HT1A agonist anxiolytic azapirones have a common alpha 2-adrenoceptor antagonist metabolite, 1-(2-pyrimidinyl)-piperazine (1PP), we measured central and peripheral alpha 2-adrenoceptor dependent responses before and after intravenous administration of 0.15 mg clonidine when healthy subjects were taking buspirone
A Gobert et al.
Neuroscience, 93(4), 1251-1262 (1999-09-29)
The serotonin1A receptor partial agonist, buspirone, also displays antagonist properties at D2 receptors and is metabolized to the alpha2-adrenergic receptor antagonist, 1-(2-pyrimidinyl-piperazine). Herein, we examined mechanisms underlying the influence of buspirone alone, and in association with the serotonin reuptake inhibitor
Lijuan Zhang et al.
Proteomics, 9(16), 4093-4097 (2009-08-07)
A novel strategy based on carboxy group derivatization is presented for specific characterization of phosphopeptides. By tagging the carboxy group with 1-(2-pyrimidyl) piperazine (PP), the ion charge states of phosphopeptides can be largely enhanced, showing great advantages for sequencing phosphorylated
L L von Moltke et al.
Psychopharmacology, 140(3), 293-299 (1999-01-07)
Biotransformation of gepirone to its principal metabolite, 1-(2-pyrimidinyl)-piperazine (1-PP), was studied in human liver microsomes and in microsomes from cDNA-transfected human lymphoblastoid cells. Formation of 1-PP from gepirone in liver microsomes proceeded with a mean apparent Km ranging from 335

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