137499
3,4-Dimethylanisole
99%
์กฐ์ง ๋ฐ ๊ณ์ฝ ๊ฐ๊ฒฉ์ ๋ณด๋ ค๋ฉด ๋ก๊ทธ์ธ๋ฅผ ํด๋ฆญํฉ๋๋ค.
ํฌ๊ธฐ ์ ํ
์ ํ์ ๋ณด (DICE ๋ฐฐ์ก ์ ๋น์ฉ ๋ณ๋)
Linear Formula:
(CH3)2C6H3OCH3
CAS ๋ฒํธ:
Molecular Weight:
136.19
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
225-142-2
MDL number:
Assay:
99%
Form:
liquid
๊ธฐ์ ์๋น์ค
๋์์ด ํ์ํ์ ๊ฐ์? ์ ํฌ ์๋ จ๋ ๊ณผํ์ ํ์ด ๋์๋๋ฆฌ๊ฒ ์ต๋๋ค.
๋์ ๋ฌธ์๊ธฐ์ ์๋น์ค
๋์์ด ํ์ํ์ ๊ฐ์? ์ ํฌ ์๋ จ๋ ๊ณผํ์ ํ์ด ๋์๋๋ฆฌ๊ฒ ์ต๋๋ค.
๋์ ๋ฌธ์form
liquid
InChI key
LVUBSVWMOWKPDJ-UHFFFAOYSA-N
InChI
1S/C9H12O/c1-7-4-5-9(10-3)6-8(7)2/h4-6H,1-3H3
SMILES string
COc1ccc(C)c(C)c1
assay
99%
refractive index
n20/D 1.517 (lit.)
bp
200-201 ยฐC (lit.)
density
0.974 g/mL at 25 ยฐC (lit.)
Quality Level
๊ด๋ จ ์นดํ ๊ณ ๋ฆฌ
Application
3,4-Dimethylanisole was used as starting reagent in the synthesis of 3- and 4-methoxy-N-hydroxyphthalimide.
์ ์ฅ ๋ฑ๊ธ
10 - Combustible liquids
wgk
WGK 3
flash_point_f
168.8 ยฐF - closed cup
flash_point_c
76 ยฐC - closed cup
๊ฐ์ฅ ์ต์ ๋ฒ์ ์ค ํ๋๋ฅผ ์ ํํ์ธ์:
์ด ์ ํ์ ์ด๋ฏธ ๊ฐ์ง๊ณ ๊ณ์ญ๋๊น?
๋ฌธ์ ๋ผ์ด๋ธ๋ฌ๋ฆฌ์์ ์ต๊ทผ์ ๊ตฌ๋งคํ ์ ํ์ ๋ํ ๋ฌธ์๋ฅผ ์ฐพ์๋ณด์ธ์.
N-Hydroxyphthalimide/Cobalt (II) Catalyzed Low Temperature Benzylic Oxidation Using Molecular Oxygen.
Wentzel BB, et al.
Tetrahedron, 56(39), 7797-7803 (2000)
Kamila K Mentel et al.
Nature communications, 9(1), 2903-2903 (2018-07-27)
Electron transfer reactions are arguably the simplest chemical reactions but they have not yet ceased to intrigue chemists. Charge-separation and charge-recombination reactions are at the core of life-sustaining processes, molecular electronics and solar cells. Intramolecular electron donor-acceptor systems capture the
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