跳转至内容
Merck

339636

Sigma-Aldrich

外-N-羟基-7-氧杂二环[2.2.1]庚-5-烯-2,3-二甲酰亚胺

98%

登录查看公司和协议定价


About This Item

经验公式(希尔记法):
C8H7NO4
CAS号:
分子量:
181.15
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:

化驗

98%

mp

194 °C (dec.) (lit.)

溶解度

THF: soluble 10 mg/mL, clear, colorless

SMILES 字串

ON1C(=O)[C@H]2C3OC(C=C3)[C@H]2C1=O

InChI

1S/C8H7NO4/c10-7-5-3-1-2-4(13-3)6(5)8(11)9(7)12/h1-6,12H/t3-,4+,5?,6?

InChI 密鑰

PPVGNPSAUJFBJY-LAXKNYFCSA-N

一般說明

exo-N-Hydroxy-7-oxabicyclo[2.2.1]hept-5-ene-2,3-dicarboximide undergoes cross-coupling with aryl boronic acid for ROMP-based O-alkylhydroxylamine parallel synthesis.

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


从最新的版本中选择一种:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本?

如果您需要特殊版本,可通过批号或批次号查找具体证书。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

Jamerson Carneiro de Oliveira et al.
Carbohydrate polymers, 250, 116966-116966 (2020-10-15)
The Diels-Alder reaction is a promising click chemistry for the design of advanced materials from cellulose nanocrystals (CNCs). Transferring such chemistry to cellulose nanocrystals requires the precise grafting of reactive Diels-Alder moeities under heterogeneous conditions without compromising the nanocrystals morphology.
Florence S Gaucher-Wieczorek et al.
Journal of combinatorial chemistry, 12(5), 655-658 (2010-09-14)
The parallel synthesis of O-aryloxyamines remains an unfulfilled need in the field of medicinal chemistry and fragment-based approaches. To fill this gap a solution-phase two-step process based on (1) a copper-catalyzed cross-coupling of aryl boronic acids with a fluorous tagged

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