205249
二碳酸二叔丁酯
99%, for peptide synthesis, ReagentPlus®
别名:
二叔丁基二碳酸酯, 焦碳酸二叔丁酯
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关于此项目
线性分子式:
[(CH3)3COCO]2O
化学文摘社编号:
分子量:
218.25
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352302
EC Number:
246-240-1
MDL number:
Beilstein/REAXYS Number:
1911173
产品名称
二碳酸二叔丁酯, ReagentPlus®, 99%
InChI key
DYHSDKLCOJIUFX-UHFFFAOYSA-N
InChI
1S/C10H18O5/c1-9(2,3)14-7(11)13-8(12)15-10(4,5)6/h1-6H3
SMILES string
CC(C)(C)OC(=O)OC(=O)OC(C)(C)C
product line
ReagentPlus®
assay
99%
form
solid or liquid
refractive index
n20/D 1.409 (lit.)
bp
56-57 °C/0.5 mmHg (lit.)
mp
23 °C (lit.)
density
0.95 g/mL at 25 °C (lit.)
application(s)
peptide synthesis
functional group
carbonate
storage temp.
2-8°C
Quality Level
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Application
Boc保护胺制备溶剂。
Tris-Boc保护的肼可在显色试剂中制备Fmoc酯以监测固相醛。
使用Synple自动合成平台(SYNPLE-SC002)、Boc保护试剂盒((SYNPLE-B001)、(SYNPLE-B002)和Boc脱保护试剂盒(SYNPLE-B011)，可自动进行Boc保护和脱保护
使用Synple自动合成平台(SYNPLE-SC002)、Boc保护试剂盒((SYNPLE-B001)、(SYNPLE-B002)和Boc脱保护试剂盒(SYNPLE-B011)，可自动进行Boc保护和脱保护
用于引入Boc保护基的试剂。
通过 Lewis 酸催化作用可以保护叔丁氧羰基衍生物等醇类。
通过叔丁氧羰基氨基丙炔与甲醛、二异丙胺以及溴化铜的反应来制备氨甲基丙二烯，是许多牛血浆胺氧化酶灭活剂的组分。
Disclaimer
水解为叔丁醇和 CO2；暴露在潮湿环境中会导致瓶内压力增大。
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Danger
Hazard Classifications
Acute Tox. 1 Inhalation - Eye Dam. 1 - Flam. Liq. 3 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
target_organs
Respiratory system
存储类别
3 - Flammable liquids
wgk
WGK 3
flash_point_f
98.6 °F - closed cup
flash_point_c
37 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
非剧毒-急性毒性1
此项目有
Simon K Shannon et al.
The Journal of organic chemistry, 69(14), 4586-4594 (2004-07-03)
A direct method for quantifying solid-phase aldehydes has been developed, using a new reagent, 4-(9-fluorenylmethyloxycarbonyl)phenylhydrazine (FmPH). The FmPH reagent was synthesized in three steps (24% overall yield) from commercially available p-hydrazinobenzoic acid. Resin-bound aldehydes reacted quantitatively with FmPH, in the
Synthetic Communications, 23, 1443-1443 (1993)
Chunhua Qiao et al.
Journal of the American Chemical Society, 126(25), 8038-8045 (2004-06-24)
Propargylic and activated allylic amines are known to inactivate the quinone-dependent plasma amine oxidases, possibly through active-site modification by the alpha,beta-unsaturated aldehyde turnover products. Although homopropargylamine (1-amino-3-butyne, 1) is a nonobvious candidate as a mechanism-based inhibitor, 1 was found to
Synlett, 2104-2104 (2006)
Hans Peter Reisenauer et al.
Angewandte Chemie (International ed. in English), 53(44), 11766-11771 (2014-09-10)
Carbonic acid (H2CO3), an essential molecule of life (e.g., as bicarbonate buffer), has been well characterized in solution and in the solid state, but for a long time, it has eluded its spectral characterization in the gas phase owing to
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