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273104

3,5-Di-tert-butylaniline

98%

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About This Item

Linear Formula:
[(CH3)3C]2C6H3NH2
CAS Number:
2380-36-1
Molecular Weight:
205.34
NACRES:
NA.22
PubChem Substance ID:
24856530
UNSPSC Code:
12352100
EC Number:
219-173-0
MDL number:
MFCD00134096
Assay:
98%
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assay

98%

mp

54-57 °C (lit.)

SMILES string

CC(C)(C)c1cc(N)cc(c1)C(C)(C)C

InChI

1S/C14H23N/c1-13(2,3)10-7-11(14(4,5)6)9-12(15)8-10/h7-9H,15H2,1-6H3

InChI key

MJKNHXCPGXUEDO-UHFFFAOYSA-N

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.

pictograms

Exclamation mark
GHS07

signalword

Warning

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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Certificates of Analysis (COA)

Lot/Batch Number
04614HE
S36206
09608CE
S34502
18314MA

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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.
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)
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Global Trade Item Number

SKUGTIN
273104-1G04061825770772