487368
4-苄氧基苯异氰酸酯
98%
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关于此项目
线性分子式:
C6H5CH2OC6H4NCO
化学文摘社编号:
分子量:
225.24
UNSPSC Code:
12352100
PubChem Substance ID:
MDL number:
assay
98%
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
SMILES string
O=C=Nc1ccc(OCc2ccccc2)cc1
InChI key
HFIHSWMJFCMLJE-UHFFFAOYSA-N
bp
129 °C/0.2 mmHg (lit.)
mp
60-62 °C (lit.)
storage temp.
2-8°C
General description
4-(Benzyloxy)phenyl isocyanate, also known as 1-(benzyloxy)-4-isocyanatobenzene, is an organic building block containing an isocyanate group.
Application
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:
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
signalword
Danger
Hazard Classifications
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
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
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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
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
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