推荐产品
化驗
98%
形狀
liquid
折射率
n20/D 1.445 (lit.)
bp
118-119 °C/753 mmHg (lit.)
密度
0.844 g/mL at 25 °C (lit.)
SMILES 字串
CC1CCCCN1
InChI
1S/C6H13N/c1-6-4-2-3-5-7-6/h6-7H,2-5H2,1H3
InChI 密鑰
NNWUEBIEOFQMSS-UHFFFAOYSA-N
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應用
通过定向过渡金属催化的sp3 C-H活化进行哌啶C-2芳基化的反应物
用于合成以下物质的反应物：
用于合成以下物质的反应物：
- 通过两步[5+2]成环反应合成氮杂环庚
- 2-氨基苯并恶唑
- 不对称取代脲
- 促肾上腺皮质激素释放因子受体1型拮抗剂
- 具有抗肿瘤活性的吉非替尼类似物
訊號詞
Danger
危險分類
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B
儲存類別代碼
3 - Flammable liquids
水污染物質分類（WGK）
WGK 3
閃點（°F）
50.0 °F - closed cup
閃點（°C）
10 °C - closed cup
個人防護裝備
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
其他客户在看
C-2 arylation of piperidines through directed transition-metal-catalyzed sp3 C-H activation.
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A novel series of [6-chloro-2-trifluoromethyl-7-aryl-7H-imidazo[1,2-a]imidazol-3-ylmethyl]-dialkylamines was discovered as potent CRF(1)R antagonists. The optimization of binding affinity in the series by the parallel reaction approach is discussed herein.
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A surprisingly efficient synthesis of azepan-4-ones via a two-step [5 + 2] annulation is developed. This reaction involves a key gold catalysis and shows generally high regioselectivities and good to excellent diastereoselectivities.
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Bioorganic & medicinal chemistry, 18(11), 3812-3822 (2010-05-15)
There is an urgent need to design and develop new and more potent EGFR inhibitors with improved anti-tumor activity. Here we describe the design and synthesis of two series of 4-benzothienyl amino quinazolines as new analogues of the EGFR inhibitor
Christopher L Cioffi et al.
The Journal of organic chemistry, 75(22), 7942-7945 (2010-10-27)
The synthesis of 2-aminobenzoxazoles can be readily achieved by two versatile, one-pot procedures utilizing commercially available tetramethyl orthocarbonate or 1,1-dichlorodiphenoxymethane, an amine, and an optionally substituted 2-aminophenol. The reactions were conducted under mild conditions and provided 2-aminobenzoxazoles in modest to
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