所有图片(2)
About This Item
线性分子式:
HC≡CC6H4NH2
CAS号:
分子量:
117.15
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
推荐产品
![1,8-二氮杂双环[5.4.0]十一碳-7-烯 98%](/deepweb/assets/sigmaaldrich/product/structures/120/564/5b373e23-1624-489c-8efb-692de0f96ffb/640/5b373e23-1624-489c-8efb-692de0f96ffb.png)
![[3R(1′R,4R)]-(+)-4-乙酰氧基-3-[1-(叔丁基二甲基硅氧基)乙基]-2-氮杂环丁酮 98%](/deepweb/assets/sigmaaldrich/product/structures/346/391/4981e055-bdcd-454c-8c8f-519083b64769/640/4981e055-bdcd-454c-8c8f-519083b64769.png)
质量水平
方案
≥98%
反应适用性
reaction type: click chemistry
储存温度
2-8°C
SMILES字符串
Nc1cccc(c1)C#C
InChI
1S/C8H7N/c1-2-7-4-3-5-8(9)6-7/h1,3-6H,9H2
InChI key
NNKQLUVBPJEUOR-UHFFFAOYSA-N
一般描述
3-乙炔苯胺是一种末端炔烃，可以通过还原3-乙炔基硝基苯进行制备。
应用
3-乙炔苯胺可用于合成以下苯并恶嗪单体：
- 双{4-[3-(3-乙炔基苯基)(2H,4H-苯并[3,4-e]-1,3-恶嗪-6-基氧基)]苯基}苯基膦基-1-酮
- [3-(3-乙炔基苯基)(2H,4H-苯并[3,4-e]1,3-氧氮杂全氢化-6-基)][3-(3-乙炔基苯基)(2H,4HH-苯并[3,4-e]1,3恶嗪-6-基)]苯基膦基-1-酮
- 双[3-[3-(3-乙炔基苯基)(2H,4H-苯并[3,4-e]-1,3-恶嗪-6-基)氧基]苯基膦基-1-酮
- 合成琥珀酰(间乙炔基)二苯胺和癸二(间乙炔基)二苯胺。
- 作为多步合成盐酸厄洛替尼的试剂。
- 制备3-(3-乙炔基苯基)-6-甲基-2H, 4H-苯并[e]1,3-恶嗪。
- 制备3-[3-(4-乙酰氨基-苄基)-[1,2,4]恶二唑-5-基] -N-(3-乙炔基-苯基)-丙酰胺。
警示用语：
Warning
危险分类
Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
3 - Flammable liquids
WGK
WGK 3
闪点(°F)
138.2 °F - closed cup
闪点(°C)
59 °C - closed cup
个人防护装备
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
Synthesis, analgesic and anti-inflammatory activities of novel 3-(4-acetamido-benzyl)-5-substituted-1,2,4-oxadiazoles.
Farooqui M, et al.
European Journal of Medicinal Chemistry, 44(2), 794-799 (2009)
Laura Marín-Caba et al.
Langmuir : the ACS journal of surfaces and colloids, 35(1), 203-211 (2018-12-24)
The design of versatile tools to improve cell targeting and drug delivery in medicine has become increasingly pertinent to nanobiotechnology. Biological and inorganic nanocarrier drug delivery systems are being explored, showing advantages and disadvantages in terms of cell targeting and
Modified synthesis of erlotinib hydrochloride.
Barghi L, et al.
Advanced Pharmaceutical Bulletin, 2(1), 119-122 (2012)
Preparation of 2'-aminoacetophenones: a one-pot hydration and reduction of 1-ethynyl-2-nitrobenzenes.
Bosch E and Jeffries L.
Tetrahedron Letters, 42(46), 8141-8142 (2001)
Diacetylene-Containing Polymers III. Poly (m,m'-butadiynylenesuccindianilide) and Poly (m,m'-butadiynylene sebacodianilide): Novel Materials for Preparation of Transparent Polydiacetylene Containing Films.
Fomine S and Ogawa T
Polymer Journal, 26(1), 93-98 (1994)
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系技术服务部门