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品質等級
化驗
97%
形狀
solid
SMILES 字串
CC(C)(C)OC(=O)N1CCC(N)CC1
InChI
1S/C10H20N2O2/c1-10(2,3)14-9(13)12-6-4-8(11)5-7-12/h8H,4-7,11H2,1-3H3
InChI 密鑰
LZRDHSFPLUWYAX-UHFFFAOYSA-N
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應用
4-氨基-1-Boc-哌啶可用于:
- 作为合成N-(3-(4-羟苯基)-丙烯酰基)-氨基酸类色胺的原料,该产物可用作沉默信息调节剂人2型(SIRT2)抑制剂
- 合成哌啶取代的三嗪衍生物和哌啶基氨基-二芳基嘧啶(pDAPY)衍生物,这些衍生物可作为有效的HIV-1非核苷逆转录酶抑制剂(HIV-1 NNRTIs)
通过伯胺与树脂结合型二甲磺酸盐直接成环,用于N-取代哌啶的微波辅助固相合成。
訊號詞
Danger
危險分類
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 2
閃點(°F)
Not applicable
閃點(°C)
Not applicable
個人防護裝備
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
其他客户在看
"Synthesis and biological evaluation of piperidine-substituted triazine derivatives as HIV-1 non-nucleoside reverse transcriptase inhibitors"
European Journal of Organic Chemistry, 51, 60-66 (2012)
"Novel piperidinylamino-diarylpyrimidine derivatives with dual structural conformations as potent HIV-1 non-nucleoside reverse transcriptase inhibitors"
Bioorganic & Medicinal Chemistry, 23(24), 6593-6597 (2013)
"N-(3-(4-Hydroxyphenyl)-propenoyl)-amino acid tryptamides as SIRT2 inhibitors"
Bioorganic & Medicinal Chemistry, 17(09), 2448-2451 (2007)
Journal of combinatorial chemistry, 8(1), 132-140 (2006-01-10)
The microwave-assisted solid-phase synthesis of piperazines, 3,9-diazaspiro[5.5]undecanes and 2,9-diazaspiro[5.5]undecanes is reported. The synthesis relies on the direct annulation of primary amines with resin-bound bismesylates. Critical to the success of this chemistry was the development of alpha-methyl benzyl carbamate resin linker.
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