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化驗
98%
bp
129 °C/0.2 mmHg (lit.)
mp
60-62 °C (lit.)
儲存溫度
2-8°C
SMILES 字串
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 密鑰
HFIHSWMJFCMLJE-UHFFFAOYSA-N
一般說明
4-(Benzyloxy)phenyl isocyanate, also known as 1-(benzyloxy)-4-isocyanatobenzene, is an organic building block containing an isocyanate group.
應用
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.[1]
It may be used in the synthesis of the following phenyl urea derivatives:[2]
It may be used in the synthesis of the following phenyl urea derivatives:[2]
- 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
訊號詞
Danger
危險分類
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
標靶器官
Respiratory system
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
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
Active Filters
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