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Merck
CN

374148

N-tert-Butylisopropylamine

97%

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About This Item

Linear Formula:
(CH3)3CNHCH(CH3)2
CAS Number:
Molecular Weight:
115.22
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
231-370-3
Beilstein/REAXYS Number:
1846752
MDL number:
Assay:
97%
Form:
liquid
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InChI key

ZWXQPERWRDHCMZ-UHFFFAOYSA-N

InChI

1S/C7H17N/c1-6(2)8-7(3,4)5/h6,8H,1-5H3

SMILES string

CC(C)NC(C)(C)C

assay

97%

form

liquid

bp

98 °C (lit.)

density

0.727 g/mL at 25 °C (lit.)

functional group

amine

General description

N-tert-Butylisopropylamine participates in the synthesis of hindered enamines.

pictograms

FlameCorrosion

signalword

Danger

hcodes

Hazard Classifications

Flam. Liq. 3 - Skin Corr. 1B

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

77.0 °F - closed cup

flash_point_c

25 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Regulatory Information

危险化学品
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David M Hodgson et al.
Journal of the American Chemical Society, 126(22), 6870-6871 (2004-06-04)
A new reactivity mode of lithium amides with epoxides leads to hindered enamines. The reaction of some of these enamines with unactivated primary and secondary alkyl halides is described, which expands the range of electrophiles that one can use in

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