์ฝ˜ํ…์ธ ๋กœ ๊ฑด๋„ˆ๋›ฐ๊ธฐ
Merck
๋ชจ๋“  ์‚ฌ์ง„(1)

์ฃผ์š” ๋ฌธ์„œ

464856

Sigma-Aldrich

1-(tert-Butoxycarbonyl)-2-pyrrolidinone

97%

๋™์˜์–ด(๋“ค):

1,1-Dimethylethyl 2-oxo-1-pyrrolidinecarboxylate, 1-(tert-Butoxycarbonyl)-2-oxopyrrolidine, 1-(tert-Butoxycarbonyl)pyrrolidin-2-one, 2-Oxopyrrolidine-1-carboxylic acid tert-butyl ester, N-(tert-Butoxycarbonyl)pyrrolidin-2-one, N-(tert-Butyloxycarbonyl)pyrrolidin-2-one, N-Boc-2-pyrrolidinone, N-tert-Butoxycarbonyl-2-oxopyrrolidine, tert-Butyl 2-Oxopyrrolidine-1-carboxylate

๋กœ๊ทธ์ธ์กฐ์ง ๋ฐ ๊ณ„์•ฝ ๊ฐ€๊ฒฉ ๋ณด๊ธฐ


About This Item

์‹คํ—˜์‹(Hill ํ‘œ๊ธฐ๋ฒ•):
C9H15NO3
CAS Number:
Molecular Weight:
185.22
MDL number:
UNSPSC ์ฝ”๋“œ:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

๋ถ„์„

97%

refractive index

n20/D 1.466 (lit.)

bp

100-105 ยฐC/0.5 mmHg (lit.)

density

1.086 g/mL at 25 ยฐC (lit.)

SMILES string

CC(C)(C)OC(=O)N1CCCC1=O

InChI

1S/C9H15NO3/c1-9(2,3)13-8(12)10-6-4-5-7(10)11/h4-6H2,1-3H3

InChI key

GJJYYMXBCYYXPQ-UHFFFAOYSA-N

๊ด€๋ จ ์นดํ…Œ๊ณ ๋ฆฌ

์ผ๋ฐ˜ ์„ค๋ช…

The kinetics of gas-phase elimination of 1-(tert-butoxycarbonyl)-2-pyrrolidinone has been investigated in a static system. The observed rate coefficient has been reported to be log k1(s-1) = (11.54 ยฑ 0.29) -(140.8 ยฑ 2.8)ยญkJmol-1 (2.303RT)-1.

ํ”ฝํ† ๊ทธ๋žจ

Exclamation mark

์‹ ํ˜ธ์–ด

Warning

์œ ํ•ด ๋ฐ ์œ„ํ—˜ ์„ฑ๋ช…์„œ

์˜ˆ๋ฐฉ์กฐ์น˜ ์„ฑ๋ช…์„œ

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

ํ‘œ์  ๊ธฐ๊ด€

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point (ยฐF)

235.4 ยฐF - closed cup

Flash Point (ยฐC)

113 ยฐC - closed cup

๊ฐœ์ธ ๋ณดํ˜ธ ์žฅ๋น„

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


๊ฐ€์žฅ ์ตœ์‹  ๋ฒ„์ „ ์ค‘ ํ•˜๋‚˜๋ฅผ ์„ ํƒํ•˜์„ธ์š”:

์‹œํ—˜ ์„ฑ์ ์„œ(COA)

Lot/Batch Number

์ ํ•ฉํ•œ ๋ฒ„์ „์„ ์ฐพ์„ ์ˆ˜ ์—†์œผ์‹ ๊ฐ€์š”?

ํŠน์ • ๋ฒ„์ „์ด ํ•„์š”ํ•œ ๊ฒฝ์šฐ ๋กœํŠธ ๋ฒˆํ˜ธ๋‚˜ ๋ฐฐ์น˜ ๋ฒˆํ˜ธ๋กœ ํŠน์ • ์ธ์ฆ์„œ๋ฅผ ์ฐพ์„ ์ˆ˜ ์žˆ์Šต๋‹ˆ๋‹ค.

์ด ์ œํ’ˆ์„ ์ด๋ฏธ ๊ฐ€์ง€๊ณ  ๊ณ„์‹ญ๋‹ˆ๊นŒ?

๋ฌธ์„œ ๋ผ์ด๋ธŒ๋Ÿฌ๋ฆฌ์—์„œ ์ตœ๊ทผ์— ๊ตฌ๋งคํ•œ ์ œํ’ˆ์— ๋Œ€ํ•œ ๋ฌธ์„œ๋ฅผ ์ฐพ์•„๋ณด์„ธ์š”.

๋ฌธ์„œ ๋ผ์ด๋ธŒ๋Ÿฌ๋ฆฌ ๋ฐฉ๋ฌธ

Kinetics of elimination of several heterocyclic carbamates in the gas phase.
Brusco Y, et al.
Journal of Physical Organic Chemistry, 15(12), 796-800 (2002)

์ž์‚ฌ์˜ ๊ณผํ•™์žํŒ€์€ ์ƒ๋ช… ๊ณผํ•™, ์žฌ๋ฃŒ ๊ณผํ•™, ํ™”ํ•™ ํ•ฉ์„ฑ, ํฌ๋กœ๋งˆํ† ๊ทธ๋ž˜ํ”ผ, ๋ถ„์„ ๋ฐ ๊ธฐํƒ€ ๋งŽ์€ ์˜์—ญ์„ ํฌํ•จํ•œ ๋ชจ๋“  ๊ณผํ•™ ๋ถ„์•ผ์— ๊ฒฝํ—˜์ด ์žˆ์Šต๋‹ˆ๋‹ค..

๊ณ ๊ฐ์ง€์›ํŒ€์œผ๋กœ ์—ฐ๋ฝ๋ฐ”๋ž๋‹ˆ๋‹ค.