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Merck
CN

487368

4-苄氧基苯异氰酸酯

98%

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线性分子式:
C6H5CH2OC6H4NCO
化学文摘社编号:
分子量:
225.24
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
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方案

98%

沸点

129 °C/0.2 mmHg (lit.)

mp

60-62 °C (lit.)

储存温度

2-8°C

SMILES字符串

O=C=Nc1ccc(OCc2ccccc2)cc1

InChI

1S/C14H11NO2/c16-11-15-13-6-8-14(9-7-13)17-10-12-4-2-1-3-5-12/h1-9H,10H2

InChI key

HFIHSWMJFCMLJE-UHFFFAOYSA-N

一般描述

4-(Benzyloxy)phenyl isocyanate, also known as 1-(benzyloxy)-4-isocyanatobenzene, is an organic building block containing an isocyanate group.

应用

4-(Benzyloxy)phenyl isocyanate may be used in the synthesis of 1,3,5-tris(4-benzyloxyphenyl)-1,3,5-triazinane-2,4,6-trione via cyclotrimerization.
It may be used in the synthesis of the following phenyl urea derivatives:
  • 1-[4-(benzyloxy)phenyl]-3-(1-methyl-3-phenyl-1H-pyrazol-5-yl)urea
  • 1-[4-(benzyloxy)phenyl]-3-[3-(4-chlorophenyl)-1-phenyl-1H-pyrazol-5-yl]urea
  • 1-[4-(benzyloxy)phenyl]-3-[3-(2-chlorophenyl)-1-phenyl-1H-pyrazol-5-yl]urea
  • N-[4-[3-[4-(benzyloxy)phenyl]ureido]phenyl]nicotinamide
  • 1-[4-(benzyloxy)phenyl]-3-(1-nicotinoylindolin-5-yl)urea
  • 4-[3-[4-(benzyloxy)phenyl]ureido]-N-phenylbenzamide

象形图

Health hazardExclamation mark

警示用语:

Danger

危险分类

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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历史批次信息供参考:

分析证书(COA)

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Bhasker Bantu et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 15(13), 3103-3109 (2009-02-13)
Catalytic rivals: Both CO(2)-protected tetrahydropyrimidin-2-ylidene-based N-heterocyclic carbenes (NHCs) and Sn(II)-1,3-dimesitylimidazol-2-ylidene, as well as Sn(II)-1,3-dimesitylimidazolin-2-ylidene complexes (example displayed), have been identified as truly latent catalysts for polyurethane (PUR) synthesis rivaling all existing systems both in activity and latency.A series of CO(2)-protected
Gustav Boije af Gennäs et al.
ChemMedChem, 6(9), 1680-1692 (2011-07-02)
In anaplastic large-cell lymphomas, chromosomal translocations involving the kinase domain of anaplastic lymphoma kinase (ALK), generally fused to the 5' part of the nucleophosmin gene, produce highly oncogenic ALK fusion proteins that deregulate cell cycle, apoptosis, and differentiation in these

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