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About This Item
线性分子式:
H3CSC6H4MgBr
CAS号:
分子量:
227.40
MDL编号:
UNSPSC代码:
12352103
PubChem化学物质编号:
NACRES:
NA.22
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反应适用性
reaction type: Grignard Reaction
浓度
0.5 M in THF
沸点
65 °C
密度
0.965 g/mL at 25 °C
储存温度
2-8°C
SMILES字符串
CSc1ccc([Mg]Br)cc1
InChI
1S/C7H7S.BrH.Mg/c1-8-7-5-3-2-4-6-7;;/h3-6H,1H3;1H;/q;;+1/p-1
InChI key
SSVQCUSLJVVRCA-UHFFFAOYSA-M
应用
4-Thioanisolemagnesium bromide can be used to prepare:
- 3,3-Ethylenedioxy-5a-hydroxy-11b-[4-(thiomethoxy)phenyl]-estr-9-en-17-one, a key intermediate for the synthesis of mifepristone analogs.
- (1S)-1,4-Anhydro-2,3,5,6-tetra-O-benzyl-1-C-[4-chloro-3-(4-methylthiobenzyl)-phenyl]-D-glucitol, a key intermediate for the synthesis of aryl D-glucofuranosides as potent hSGLT2 and hSGLT1 inhibitors.
法律信息
Rieke® Metals, Inc. 的产品，®Rieke Metals, Inc. 的注册商标
警示用语：
Danger
危险分类
Acute Tox. 4 Oral - Carc. 2 - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B - STOT SE 3
靶器官
Central nervous system, Respiratory system
补充剂危害
储存分类代码
3 - Flammable liquids
WGK
WGK 3
闪点(°F)
1.4 °F
闪点(°C)
-17 °C
法规信息
新产品
Tzung-Sheng Lin et al.
Bioorganic & medicinal chemistry, 21(21), 6282-6291 (2013-09-28)
Novel C-aryl-d-glucofuranosides were synthesized and evaluated for their capacity to inhibit human sodium-dependent glucose co-transporter 2 (hSGLT2) and hSGLT1. Compound 21q demonstrated the best in vitro inhibitory activity against SGLT2 in this series (EC50=0.62μM).
Weiqin Jiang et al.
Steroids, 71(11-12), 949-954 (2006-08-29)
A novel series of steroidal compounds were designed and synthesized with various phosphorus-containing groups on the 17beta-side chain as progesterone receptor antagonists. The structure-activity relationships of these compounds are discussed. Selected compounds were tested in an rat progesterone-sensitive assay. Some
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