您当前所在的位置:首页 > 产品中心 > 产品信息
Deoxo-Fluor® 溶液_分子结构_CAS_202289-38-1)
点击图片或这里关闭

Deoxo-Fluor® 溶液

产品号 94327 公司名称 Sigma Aldrich
CAS号 202289-38-1 公司网站 http://www.sigmaaldrich.com
分子式 C6H14F3NO2S 电 话 1-800-521-8956
分子量 221.2410696 传 真
纯 度 电子邮件
保 存 Chembase数据库ID: 9793

产品价格信息

请登录

产品别名

标题
Deoxo-Fluor® solution
IUPAC标准名
bis(2-methoxyethyl)(trifluoro-λ4-sulfanyl)amine
IUPAC传统名
bis(2-methoxyethyl)(trifluoro-λ4-sulfanyl)amine
别名
双(2-甲氧基乙基)氨基三氟化硫 溶液
Bis(2-methoxyethyl)aminosulfur trifluoride solution

产品登记号

PubChem SID 24889985
CAS号 202289-38-1
MDL号 MFCD01321415

产品性质

浓度 50% in THF
Empirical Formula (Hill Notation) C6H14F3NO2S
密度 1.03-1.05 g/mL at 20 °C
闪点 <10 °C
闪点 <50 °F
GHS危险品标识 GHS02
GHS危险品标识 GHS05
GHS危险品标识 GHS06
GHS警示词 Danger
GHS危险声明 H225-H261-H301 + H331-H314-H335
欧盟危险性物质标志 易燃性(Flammable) 易燃性(Flammable) (F)
欧盟危险性物质标志 有毒(Toxic) 有毒(Toxic) (T)
MSDS下载 下载链接
个人保护装置 Faceshields, full-face respirator (US), Gloves, Goggles, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
GHS警示性声明 P210-P231 + P232-P261-P280-P301 + P310-P422
RID/ADR UN 3286 3/PG 2
危险公开号 11-14-19-23/25-29-35-37
安全公开号 16-26-36/37/39-45
保存温度 2-8°C
欧盟补充危害声明 Contact with water liberates toxic gas., May form explosive peroxides., Reacts violently with water.
联合国危险货物等级 3
联合国危险货物编号 3286
联合国危险货物包装类别(PG) 2
德国WGK号 3

产品详细信息

详细说明 (English)
Other Notes
Fluorinating agent with high thermal stability7,8,9
Packaging
10, 50 mL in PFA/FEP bottle
Application
Reactant for:
• Fluorination reactions1
• Preparation of fluorinated catechols via Umpolung based nucleophilic deoxyfluorination2
• Preparation of imidazole derivatives as CXCR3 antagonists3
• Ring expansion reactions4
• Synthesis of acyl azides from carboxylic acids5
• Aldehydes or ketones from carboxylic acids and Grignard reagents via in situ generation of Weinreb amides6
Legal Information
Deoxo-Fluor is a registered trademark of Air Products & Chemicals, Inc.
详细说明 (简体中文)
Other Notes
具有高热稳定性的氟化剂7,8,9
包装
10, 50 mL in PFA/FEP btl
Application
Reactant for:
• Fluorination reactions1
• Preparation of fluorinated catechols via Umpolung based nucleophilic deoxyfluorination2
• Preparation of imidazole derivatives as CXCR3 antagonists3
• Ring expansion reactions4
• Synthesis of acyl azides from carboxylic acids5
• Aldehydes or ketones from carboxylic acids and Grignard reagents via in situ generation of Weinreb amides6
法律信息
Deoxo-Fluor 注册商标 Air Products & Chemicals, Inc.

参考文献