추천 제품
Quality Level
분석
98%
mp
160-163 °C (lit.)
SMILES string
CC(C)(C)c1ccc(O)c(N)c1
InChI
1S/C10H15NO/c1-10(2,3)7-4-5-9(12)8(11)6-7/h4-6,12H,11H2,1-3H3
InChI key
RPJUVNYXHUCRMG-UHFFFAOYSA-N
애플리케이션
2-Amino-4-tert-butylphenol can be used as a reactant to prepare:
- 4-tert-butyl-2-[(pyridylmethylene)amino]phenol intermediates, which are used to synthesize biologically important 2-(pyridyl)benzoxazole derivatives.
- Prolinamide phenols, as efficient hydrophobic organocatalysts for direct asymmetric aldol reaction aldehydes and ketones in water.
- N-(2-hydroxy-4-tert-butylphenyl)-acetamide, a key intermediate to prepare uranylsalophene derivatives which can be used as selective receptors in anion sensitive membrane sensors.
- Poly(2-amino-4-tert-butylphenol) [poly(2A-4TBP)] by electrochemical or chemical oxidative polymerization reaction.
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
The chemical and electrochemical oxidative polymerization of 2-amino-4-tert-butylphenol
Electrochimica Acta, 212, 958-965 (2016)
Synthesis of 2-(2-, 3-, and 4-pyridyl) benzoxazoles by the reaction of phenolic Schiff bases with thianthrene cation radical.
Journal of Heterocyclic Chemistry, 39(6), 1279-1282 (2002)
Rationally designed 4-phenoxy substituted prolinamide phenols organocatalyst for the direct aldol reaction in water.
Tetrahedron Letters, 50(11), 1173-1176 (2009)
Neutral anion receptors: synthesis and evaluation as sensing molecules in chemically modified field effect transistors.
The Journal of Organic Chemistry, 62(26), 9034-9038 (1997)
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