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N,N-Dimethylformamide dineopentyl acetal was used in the esterification of Nα-9-fluorenylmethyloxycarbonylamino acids(Fmoc). It was used in the synthesis of 1,3-dialkyl, benzyl and cyclohexyl barbiturate derivatives. It was used as reagent during the synthesis of L-serine and L-cystine stereospecifically labeled with deuterium at the β-position.
シグナルワード
Warning
危険有害性情報
危険有害性の分類
Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
ターゲットの組織
Respiratory system
保管分類コード
3 - Flammable liquids
WGK
WGK 3
引火点(°F)
125.6 °F - closed cup
引火点(℃)
52 °C - closed cup
個人用保護具 (PPE)
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
消防法
第4類:引火性液体
第二石油類
危険等級III
非水溶性液体
Jan Code
140244-10G:
140244-VAR:
140244-50G:
140244-BULK:
Clinical toxicology, 16(2), 189-199 (1980-04-01)
Procedures are described for the on-column gas chromatographic synthesis of various N-alkyl-N-alkyl barbiturates where groups added to the nitrogens are benzyl, cyclohexyl, or straight chains with 1 to 10 carbons. The 1,3-dialkyl barbiturates having methyl, ethyl, n-propyl, n-butyl, cyclohexyl, isopropyl
International journal of peptide and protein research, 23(4), 342-349 (1984-04-01)
The attachment of Fmoc-amino acids onto p- alkoxybenzyl alcohol resins via DCC-DMAP coupling suffers from two different problems: formation of dimers and racemization. The use of N,N-dimethylformamide dineopentyl acetal for the preparation of Fmoc- aminoacyloxybenzyl handles is the basis of
Preparation of l-serine and l-cystine stereospecifically labeled with deuterium at the ?-position.
Tetrahedron Asymmetry, 17(12), 1890-1894 (2006)
International journal of peptide and protein research, 26(1), 92-97 (1985-07-01)
Several Fmoc-amino acids have been esterified by use of N,N-dimethylformamide dineopentyl acetal to 2,4,5-trichlorophenyl 3'-(4''-hydroxymethyl-phenoxy)propionate, and the resultant handle derivatives were purified and then quantitatively coupled onto aminomethyl supports. Compared to literature methodology, the present procedure is preferred because: (i)
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