所有图片(2)
About This Item
经验公式（希尔记法）:
C5H10Cl2N2
CAS号:
分子量:
169.05
MDL编号:
UNSPSC代码:
12352005
PubChem化学物质编号:
NACRES:
NA.22
推荐产品
产品名称
2-氯-1,3-二甲基氯化咪唑啉,
表单
crystalline
质量水平
反应适用性
reaction type: Coupling Reactions
mp
133-140 °C (lit.)
应用
peptide synthesis
官能团
chloro
SMILES字符串
[Cl-].CN1CC[N+](C)=C1Cl
InChI
1S/C5H10ClN2.ClH/c1-7-3-4-8(2)5(7)6;/h3-4H2,1-2H3;1H/q+1;/p-1
InChI key
AEBBXVHGVADBHA-UHFFFAOYSA-M
应用
合成试剂：
标记葡萄糖作为支链寡糖合成的中间体
荧光化学传感器
1,2-二胺作为共激活剂相关精氨酸甲基转移酶 1 的抑制剂
变构葡萄糖激酶激活剂
用于合成以下物质的反应物：
伯胺中的有机叠氮化物
aza-Henry 反应试剂
标记葡萄糖作为支链寡糖合成的中间体
荧光化学传感器
1,2-二胺作为共激活剂相关精氨酸甲基转移酶 1 的抑制剂
变构葡萄糖激酶激活剂
用于合成以下物质的反应物：
伯胺中的有机叠氮化物
aza-Henry 反应试剂
用于 macroviracin A、cycloviracin B1 和环硅烷全合成的活化剂。
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
Alois Fürstner et al.
Journal of the American Chemical Society, 125(43), 13132-13142 (2003-10-23)
The first total synthesis of the antivirally active glycolipid cycloviracin B(1) (1) is described. The approach is based on a two-directional synthesis strategy which constructs the C(2)()-symmetrical macrodiolide core of the target by an efficient template-directed macrodilactonization reaction promoted by
Journal of Organometallic Chemistry, 686, 175-182 (2003)
Yanzi Gou et al.
Journal of polymer science. Part A, Polymer chemistry, 51(12), 2588-2597 (2013-06-14)
Synthetic glycopolymers are important natural oligosaccharides mimics for many biological applications. To develop glycopolymeric drugs and therapeutic agents, factors that control the receptor-ligand interaction need to be investigated. A library of well-defined glycopolymers has been prepared by the combination of
Shunya Takahashi et al.
The Journal of organic chemistry, 69(13), 4509-4515 (2004-06-19)
The C(2)-symmetric macrodiolide core 2 of an antiviral agent, macroviracin A (1), was constructed in a single step by the intermolecular macrodimerization of C(22)-hydroxy carboxylic acid 3 with 2-chloro-1,3-dimethylimidazolinium chloride and DMAP in the presence of sodium hydride (NaH). The
Shonoi A Ming et al.
Glycobiology, 28(2), 100-107 (2017-12-12)
Neisseria meningitidis Group X is an emerging cause of bacterial meningitis in Sub-Saharan Africa. The capsular polysaccharide of Group X is a homopolymer of N-acetylglucosamine α(1-4) phosphate and is a vaccine target for prevention of disease associated with this meningococcal
商品
N-Acylimidazoles and carbonylimidazoles are reactive intermediates used for amino compound acylation, surpassing DCC as coupling reagents.
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