- 询价
- Elucigen
- 中国
- PBN2011089
- 2025年07月12日
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3-cyanocyclobutane-1-carboxylic acid
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tert-butyl (3aS,6aR)-3a-fluoro-1,2,3,4,6,6a-hexahydropyrrolo[3,4-c]pyrrole-5-carboxylate hydrochloride
询价4-tert-butyl-3-fluoro-aniline
询价tert-butyl N-{9-[(3aR,4R,6R,6aR)-6-(hydroxymethyl)-2,2-dimethyl-tetrahydro-2H-furo[3,4-d][1,3]dioxol-4-yl]-9H-purin-6-yl}-N-[(tert-butoxy)carbonyl]carbamate
询价1-methylcyclobutane-1,3-diol
询价
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- 详细信息
- 文献和实验
- 技术资料
- 保存条件：
Recommended Temperature controlled NMT30℃ for storage, Protected by Nitrogen
- 英文名：
tert-butyl N-methyl-N-[(3R)-pyrrolidin-3-yl]carbamate
- 供应商：
南京鼎石
- CAS号：
392338-15-7
- 规格：
10g///25g///50g///100g///250g///500g///1kg///5kg///27135kg
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文献和实验RNA Synthesis Using 2-O-(Tert-Butyldimethylsilyl) Protection
This chapter enables the reader to carry out the solid-phase synthesis of ribonucleic acid (RNA) using β-cyanoethyl phosphoramidite chemistry combined with tert -butyldimethylsilyl protection of the ribose 2′-hydroxyl group. Phosphoramidite
Synthesis of Peptides Using Tert-Butyloxycarbonyl (Boc) as the -Amino Protection Group
The use of the tert -butyloxycarbonyl (Boc) as the N α-amino protecting group in peptide synthesis can be advantageous in several cases, such as synthesis of hydrophobic peptides and peptides containing ester and thioester moieties
-4-sulfonate (15 ,16 ), methyl 4-(6-methoxynaphthalene-2-yl)-4-oxo-2-butenoate (17 ), N-(1-pyrenyl)maleimide (18 ), monobromobimane (19 –23 ), o -phthaldialdehyde (24 ,25 ), 9-fluorenylmethyloxycarbonyl chloride (26 ), and 2-chloro-1-methylpyridinium
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