规格 | 目录价格 | 上海 | 安徽 | 武汉 | 成都 | 北方 | 深圳 | 会员价格 | 数量 |
---|---|---|---|---|---|---|---|---|---|
25g | ¥ ÈķĬÑÑ | > 10 | > 10 | 7 | > 10 | > 10 | > 10 | ¥ ÈķĬÑÑ | - + |
100g | ¥ ķÑĬÑÑ | 4 | > 10 | > 10 | > 10 | > 10 | > 10 | ¥ ķÑĬÑÑ | - + |
500g | ¥ ƞƞķĬÑÑ | -- | > 10 | 8 | 9 | > 10 | 5 | ¥ ƞƞķĬÑÑ | - + |
1kg | ¥ ņķǔĬÑÑ | -- | > 10 | -- | 4 | 9 | 5 | ¥ ņķǔĬÑÑ | - + |
5kg | ¥ ƩķƩÑĬÑÑ | -- | > 10 | -- | -- | -- | -- | ¥ ƩķƩÑĬÑÑ | - + |
10kg | ¥ ǔƓņÑĬÑÑ | -- | > 10 | -- | -- | -- | -- | ¥ ǔƓņÑĬÑÑ | - + |
产品编号
1036325
CAS 号
57260-71-6
中文名称
1-(叔丁氧羰基)哌嗪
MDL 号
MFCD00075265
分子量
186.25
存储条件
2-8°C
网页展示纯度为入库指导纯度值,各批次间存在一定差异,实际纯度以收货为准
熔点
43-47°C
沸点
76 °C at 0.1 mmHg
闪点
113°C
旋光
描述
TPSA
41.57
LogP
0.8267
H_Acceptors
3
H_Donors
1
Rotatable_Bonds
0
[1]. Binbin Cheng, et al. Discovery of novel resorcinol diphenyl ether-based PROTAC-like molecules as dual inhibitors and degraders of PD-L1. Eur J Med Chem. 2020;199:112377.
[2]. Akihiko Tanitame, et al. Design, synthesis and structure-activity relationship studies of novel indazole analogues as DNA gyrase inhibitors with Gram-positive antibacterial activity. Bioorg Med Chem Lett. 2004 Jun 7;14(11):2857-62.
[3]. Dengfeng Dou, et al. Inhibition of noroviruses by piperazine derivatives. Bioorg Med Chem Lett. 2012 Jan 1;22(1):377-9.
[4]. Nisar Ullah, et al. Synthesis and dual D2 and 5-HT1A receptor binding affinities of 5-piperidinyl and 5-piperazinyl-1H-benzo[d]imidazol-2(3H)-ones. J Enzyme Inhib Med Chem. 2014 Apr;29(2):281-91.
[5]. Ravi Varala, et al. Molecular iodine-catalyzed facile procedure for N-Boc protection of amines. J Org Chem. 2006 Oct 13;71(21):8283-6.
警示图
警示词
Warning
危险申明
H315-H319-H335
警告申明
P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
GHS 编码
GHS07
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现货供应
专业护航
售后无忧
品质保障
无需凑单