273104
3,5-Di-tert-butylaniline
98%
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About This Item
Linear Formula:
[(CH3)3C]2C6H3NH2
CAS Number:
Molecular Weight:
205.34
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
219-173-0
MDL number:
Product Name
3,5-Di-tert-butylaniline, 98%
assay
98%
InChI key
MJKNHXCPGXUEDO-UHFFFAOYSA-N
InChI
1S/C14H23N/c1-13(2,3)10-7-11(14(4,5)6)9-12(15)8-10/h7-9H,15H2,1-6H3
SMILES string
CC(C)(C)c1cc(N)cc(c1)C(C)(C)C
mp
54-57 °C (lit.)
Application
3,5-Di-tert-butylaniline was used in the synthesis of lipophilic wedges by reacting with 2-amino-6-chloropyrimidin-4-ol in a refluxing mixture of acetic and hydrochloric acid.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Thi Mien Trung Huynh et al.
Nanoscale, 9(1), 362-368 (2016-12-08)
Highly oriented pyrolytic graphite (HOPG) can be covalently grafted with aryl radicals generated via the electrochemical reduction of 3,5-bis-tert-butyl-diazonium cations (3,5-TBD). The structure of the grafted layer and its stability under electrochemical conditions were assessed with electrochemical scanning tunneling microscopy
JANUS WEDGES: a new approach towards nucleobase-pair recognition.
Chemical Communications (Cambridge, England), 21, 2443-2444 (1996)
Lakshya Daukiya et al.
Nanoscale, 13(5), 2972-2981 (2021-01-29)
Covalent functionalization is one of the most efficient ways to tune the properties of layered materials in a highly controlled manner. However, molecular chemisorption on semiconducting transition metal dichalcogenides remains a delicate task due to the inertness of their surface.
Ji Han Kim et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 25(38), 9060-9070 (2019-04-16)
Organic light-emitting diodes are currently under research to achieve high efficiency and long life by using thermally activated delayed fluorescence (TADF) materials. In particular, many studies have focused on ensuring high efficiency in fluorescent devices by introducing TADF materials. Herein
Gina Ambrosio et al.
Scientific reports, 10(1), 4114-4114 (2020-03-07)
Chemical reaction with diazonium molecules has revealed to be a powerful method for the surface chemical modification of graphite, carbon nanotubes and recently also of graphene. Graphene electronic structure modification using diazonium molecules is strongly influenced by graphene growth and
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