登录 查看组织和合同定价。
选择尺寸
变更视图
关于此项目
经验公式(希尔记法):
C15H23NaO
化学文摘社编号:
分子量:
242.33
UNSPSC Code:
12352111
NACRES:
NA.22
MDL number:
form
powder
Quality Level
storage temp.
−20°C
SMILES string
[Na+].[O-]c1c(cc(cc1C(C)(C)C)C)C(C)(C)C
InChI
1S/C15H24O.Na/c1-10-8-11(14(2,3)4)13(16)12(9-10)15(5,6)7;/h8-9,16H,1-7H3;/q;+1/p-1
InChI key
AOIQNBCUUALSSZ-UHFFFAOYSA-M
Application
NaBHT is an organic soluble base used for the Pd-catalyzed arylation of base-sensitve amines with aryl halides. NaBHT has also been show to be an efficient hydride source for the Pd-catalyzed reduction of aryl halides.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Sepideh Sharif et al.
Angewandte Chemie (International ed. in English), 54(33), 9507-9511 (2015-06-23)
A single set of reaction conditions for the palladium-catalyzed amination of a wide variety of (hetero)aryl halides using primary alkyl amines has been developed. By combining the exceptionally high reactivity of the Pd-PEPPSI-IPent(Cl) catalyst (PEPPSI=pyridine enhanced precatalyst preparation, stabilization, and
Sepideh Sharif et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 25(57), 13099-13103 (2019-09-21)
NaBHT (sodium butylated hydroxytoluene), a hindered and soluble base for the efficient arylation of various base-sensitive amines and (hetero)aryl halides has been found to have an unanticipated role as a hydride donor to reduce (hetero)aryl halides and allylic acetates. Mechanistic
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 912395-5G | 04061841783985 |
| 912395-1G | 04061841783978 |