6-(Benzyloxy)-3-pyridinamine(CAS番号:75926-65-7)

基本情報

6-(Benzyloxy)-3-pyridinamine

CAS番号

75926-65-7

分子式

C12H12N2O

分子量

200.24 g/mol

Quick Actions

基本的な物理特性

SMILES

C1=CC=C(C=C1)COC2=NC=C(C=C2)N

InChI

InChI=1S/C12H12N2O/c13-11-6-7-12(14-8-11)15-9-10-4-2-1-3-5-10/h1-8H,9,13H2

InChIKey

CDCFXBSOKSIQPU-UHFFFAOYSA-N

LogP

2.2428

トポロジカル極性表面積

48.14 Ų

水素結合ドナー/アクセプター

2 / 3

複雑度

181

分類と用途

安全情報

安全情報を表示

同義語と参考文献

英語

  • AKOS000137375
  • FT-0734763
  • US18128000
  • 6-[(Phenylmethyl)oxy]-3-pyridinamine
  • 5-Amino-2-benzyloxypyridine
  • NIOSH/US1812800
  • TS-02837
  • 6-benzyloxy-pyridin-3-ylamine
  • EN300-45483
  • 6-benzyloxypyridin-3-amine
  • 6-(Benzyloxy)-3-pyridinamine #
  • DTXSID10340287
  • 75926-65-7
  • CS-0021987
  • 6-(benzyloxy)pyridin-3-amine
  • SCHEMBL224083
  • F74416
  • SB78380
  • Pyridine, 5-amino-2-(benzyloxy)-
  • 6-(benzyloxy)pyridin-3-amine, AldrichCPR
  • 6-Benzyloxypyridin-3-ylamine
  • 6-phenylmethoxypyridin-3-amine
  • MFCD01692494
  • SY174142
  • 3-Pyridinamine, 6-(phenylmethoxy)-
  • 5-Amino-2-(benzyloxy)pyridine
  • 6-(Benzyloxy)pyridin-3-amine
  • 3-amino-6-(benzyloxy)pyridine
  • 6-(Benzyloxy)-3-pyridinamine
  • 6-[(phenylmethyl)oxy]-3-pyridinamine
  • 6-Benzyloxy-[3]pyridylamin
  • 6-benzyloxy-[3]pyridylamine
  • AC1Q52I4
  • SBB051835
  • SureCN224083

MDL_Number

MFCD01692494

CAS番号

75926-65-7

サプライヤー情報

サプライヤー名 会員レベル 認証状況 主要カテゴリー 最小注文数量 アクション
中国中国 - Shanghai Jieshukai Biotechnology Co., Ltd.
中国中国 - Shanghai Tengzhun BioScience Co., Ltd.
中国中国 - Hubei Hanwei Chemical Co., Ltd.
中国中国 - Shanghai Hansi Chemical Co., Ltd.
中国中国 - Sichuan Befeng Biotechnology Co., Ltd.
中国中国 - Shanghai Yuyeh Biotechnology Co., Ltd.
フランスフランス - Michel Baulé SA
日本日本 - Mitsubishi Chemical Corporation

関連論文

Vapor-fed photoelectrolysis of water at 0.3 V using gas-diffusion photoanodes of SrTiO3 layers

Hyosuke Mukohara, Hiroki Sato, Chihiro Tateishi, Hiromasa Sato

2019-12-26 Paper

DOI: 10.1039/C9SE01068H

Non-aqueous neptunium and plutonium redox behaviour in THF – access to a rare Np(iii) synthetic precursor

Nickolas H. Anderson, Suzanne C. Bart, Andrew J. Gaunt, Brian L. Scott

2018-05-08 Communication

DOI: 10.1039/C8CC02611D

Increasing efficiency of perovskite solar cells using low concentrating photovoltaic systems

Hasan Baig, Hiroyuki Kanda, Abdullah M. Asiri, Mohammad Khaja Nazeeruddin, Tapas Mallick

2019-11-18 Paper

DOI: 10.1039/C9SE00550A

Ether-functionalization of monoethanolamine (MEA) for reversible CO2 capture under solvent-free conditions with high-capacity and low-viscosity

An-Hua Liu, Jie-Jie Li, Bai-Hao Ren, Xin-Ru Sha, He Jiang, Xiao-Bing Lu

2019-12-04 Paper

DOI: 10.1039/C9SE00756C

Direct arylation polycondensation towards water/alcohol-soluble conjugated polymers as the electron transporting layers for organic solar cells

Qingwu Yin, Zhenfeng Wang, Boming Xie, Fei Huang, Yong Cao

2021-04-30 Communication

DOI: 10.1039/D1CC01128F

Development of wound healing scaffolds with precisely-triggered sequential release of therapeutic nanoparticles

Tauseef Ahmad, Sean McGrath, Catherine Sirafim, Ronaldo J. F. C. do Amaral, Shin-Loong Soong, Renuka Sitram, Shifa'a Turkistani, Francesco Santarella

2020-10-27 Paper

DOI: 10.1039/D0BM01277G

Boronic acid liposomes for cellular delivery and content release driven by carbohydrate binding‡

Xiaoyu Zhang, Daiane S. Alves, Jinchao Lou, Shelby D. Hill, Francisco N. Barrera, Michael D. Best

2018-05-21 Communication

DOI: 10.1039/C8CC00820E

High-performance tungsten carbide electrocatalysts for the hydrogen evolution reaction

Jing Li, Bao Wang, Wei Liu

2019-12-13 Communication

DOI: 10.1039/C9SE00853E

Sugar ketals as a platform molecule to overcome the limitation of converting biomass into green-hydrocarbons in a typical refinery

Matheus Souza, Joana Pinto, Laura M. Esteves, Yiu Lau Lam, Leandro Soter de Mariz e Miranda

2019-12-10 Paper

DOI: 10.1039/C9SE00379G

Tessellation strategy for the interfacial synthesis of an anthracene-based 2D polymer via [4+4]-photocycloaddition

Renzeng Chen, Danbo Wang, Wenbo Hao, Feng Shao, Yingjie Zhao

2021-05-07 Communication

DOI: 10.1039/D1CC02179F