482625
(S)-(+)-6,6′-二溴-1,1′-二-2-萘酚
98%
登录查看公司和协议定价
选择尺寸
关于此项目
线性分子式:
[BrC10H5(OH)]2
化学文摘社编号:
分子量:
444.12
MDL编号:
UNSPSC代码:
12352005
PubChem化学物质编号:
NACRES:
NA.22
方案
98%
旋光性
[α]20/D +49°, c = 1.8 in THF
mp
195-199 °C (lit.)
InChI
1S/C20H12Br2O2/c21-13-3-5-15-11(9-13)1-7-17(23)19(15)20-16-6-4-14(22)10-12(16)2-8-18(20)24/h1-10,23-24H
InChI key
OORIFUHRGQKYEV-UHFFFAOYSA-N
一般描述
(S)-(+)-6,6′-Dibromo-1,1′-bi-2-naphthol is an aromatic chiral Bronsted acid.
应用
(S)-(+)-6,6′-Dibromo-1,1′-bi-2-naphthol may be used in the synthesis of (2R,3S)-3-phenylisoserine hydrochloride. It may also be used in the synthesis of BINOL-derived chiral ligands with aryl substituents in the 6,6-positions. [BINOL=1,1′-bi-2-naphthol]
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
法规信息
新产品
此项目有
Chiral bis-trifluoromethanesulfonylamide as a chiral Br?nsted acid catalyst for the asymmetric hetero Diels-Alder reaction with Danishefsky's diene.
Tonoi T and Mikami K.
Tetrahedron Letters, 46(37), 6355-6358 (2005)
Asymmetric epoxidation of a, ?-unsaturated ketones catalyzed by chiral ytterbium complexes.
Chen R, et al.
Tetrahedron Letters, 42(39), 6919-6921 (2001)
Catalytic asymmetric synthesis of both syn-and anti-?-amino alcohols.
Kobayashi S, et al.
Journal of the American Chemical Society, 120(2), 431-432 (1998)
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.
联系客户支持