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325430

三苯甲胺

Name: 三苯甲胺
Brand: ALDRICH
Price: 5551.31 CNY

99%

别名:

三苯基甲胺

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100 μL

¥5,551.31

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100 μL

¥5,551.31

About This Item

线性分子式:

(C₆H₅)₃CNH₂

CAS号:

5824-40-8

分子量:

259.34

Beilstein:

2113674

MDL编号:

MFCD00008047

UNSPSC代码:

12352100

PubChem化学物质编号:

24859510

NACRES:

NA.22

¥5,551.31

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此商品	HPA023010	HPA018295	HPA019194
HPA008164 Anti-TSKU antibody produced in rabbit	HPA023010 Anti-TTC19 antibody produced in rabbit	HPA018295 Anti-ATXN2 antibody produced in rabbit	HPA019194 Anti-SCAMP2 antibody produced in rabbit
antibody form affinity isolated antibody	antibody form affinity isolated antibody	antibody form affinity isolated antibody	antibody form affinity isolated antibody
Quality Level 100	Quality Level 100	Quality Level -	Quality Level 100
biological source rabbit	biological source rabbit	biological source rabbit	biological source rabbit
product line Prestige Antibodies^® Powered by Atlas Antibodies	product line Prestige Antibodies^® Powered by Atlas Antibodies	product line Prestige Antibodies^® Powered by Atlas Antibodies	product line Prestige Antibodies^® Powered by Atlas Antibodies
clone polyclonal	clone polyclonal	clone polyclonal	clone polyclonal

一般描述

已对三苯基甲胺与三氟化硼的反应进行了研究。[1]

应用

三苯甲胺已被用于制备类金刚石多孔有机盐。[2]它也被用于制备N-三苯甲基化β-氨基醇，是可用于有机合成中的构成元件。[3]

象形图

GHS07

警示用语：

Warning

危险声明

H315,H319,H335

预防措施声明

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

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

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

技术规格说明书

历史批次信息供参考:

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Reaction of triphenylmethylamines with boron trihalides.

Ronan RJ, et al.

Journal of the American Chemical Society, 93(25), 6811-6814 (1971)

Role-allocated combination of two types of hydrogen bonds towards constructing a breathing diamondoid porous organic salt.

Atsushi Yamamoto et al.

Chemistry (Weinheim an der Bergstrasse, Germany), 19(9), 3006-3016 (2013-01-12)

A diamondoid porous organic salt (d-POS) composed of 8-hydroxyquinoline-5-sulfonic acid (HQS) and triphenylmethylamine (TPMA) shows reversible structure contraction and expansion ("breathing") in response to guest desorption and adsorption. This flexible structure is designed hierarchically by utilizing two different types of

Tritylamine (triphenylmethylamine) in organic synthesis; II. The reaction of tritylamine with oxiranes-synthesis of N-trityl-? aminoalcohols.

Soroka M and Goldeman W.

ARKIVOC (Gainesville, FL, United States), 12, 31-37 (2003)

Novel inhibitors of the Gardos channel for the treatment of sickle cell disease.

Grant A McNaughton-Smith et al.

Journal of medicinal chemistry, 51(4), 976-982 (2008-02-01)

Sickle cell disease (SCD) is a hereditary condition characterized by deformation of red blood cells (RBCs). This phenomenon is due to the presence of abnormal hemoglobin that polymerizes upon deoxygenation. This effect is exacerbated when dehydrated RBCs experience a loss

Structure-activity relationship of S-trityl-L-cysteine analogues as inhibitors of the human mitotic kinesin Eg5.

Salvatore Debonis et al.

Journal of medicinal chemistry, 51(5), 1115-1125 (2008-02-13)

The human kinesin Eg5 is a potential drug target for cancer chemotherapy. Eg5 specific inhibitors cause cells to block in mitosis with a characteristic monoastral spindle phenotype. Prolonged metaphase block eventually leads to apoptotic cell death. S-trityl-L-cysteine (STLC) is a

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三苯甲胺

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