物质信息

ID:329164

(4-羧丁基)三苯基溴化膦

名称和标识
IUPAC标准名
(4-carboxybutyl)triphenylphosphanium bromide
IUPAC传统名
(4-carboxybutyl)triphenylphosphanium bromide
别名
NSC 1477565-(Triphenylphosphonio)pentanoic acid bromideCarboxybutyltriphenylphosphonium bromide(4-羧丁基)三苯基溴化膦(4-Carboxybutyl)triphenylphosphonium bromide
数据登录号
Beilstein号
PubChem SID
化合物性质
产品相关信息
线性分子式
(C6H5)3P(Br)(CH2)4COOH
纯度
98%
安全信息
欧盟危险性物质标志
刺激性 刺激性 (Xi)
GHS警示性声明
P261-P305+P351+P338
危险公开号
36/37/38
德国WGK号
3
GHS警示词
Warning
GHS危险声明
H315-H319-H335
安全公开号
26-36
个人保护装置
dust mask type N95 (US), Eyeshields, Gloves
MSDS下载
GHS危险品标识
GHS07
急性毒性(口服,皮肤接触,吸入),类别4
皮肤刺激,类别2
眼刺激,类别2
皮肤过敏,类别1
特定目标器官毒性 -一次接触,类别3
理化性质
熔点
204-207 °C(lit.)
描述信息
包装
10, 50, 250 g in poly bottle
Application

• Used as a platform for delivery of pro-apoptotic peptides into the mitochondria of tumor cells1Reactant for preparation of:
• Ring skeletons via ring closing metathesis and double bond migration ring closing metathesis reactions2
• Methyl alkenyl quinolones as antimycobacterial agents3
• Prostaglandins and their drug analogs via Gold-catalyzed Meyer-Schuster rearrangement4
• Diphenylmethylpiperazines as N-type calcium channel blockers as potential therapeutic agents5
• Folate receptor-specific glycinamide ribonucleotide formyltransferase (GARFTase) inhibitors with antitumor activity6
• Cycloalkylidene alkanols with antileishmanial activity, via Wittig reaction7
分子图谱
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参考文献
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