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![1',4',6',7'-tetrahydrospiro[cyclopropane-1,5'-indazole]-3'-carboxylic acid](https://img1.dxycdn.com/p/s14/2025/0410/677/6756504026383120191.jpg!wh200)
1',4',6',7'-tetrahydrospiro[cyclopropane-1,5'-indazole]-3'-carboxylic acid
询价
tert-butyl (2S,4S)-4-cyano-2-methyl-pyrrolidine-1-carboxylate
询价2-methyl-3,4-dihydro-1H-isoquinolin-6-ol
询价2-[1-(benzyloxy)-2-methylpropan-2-yl]-6-fluoro-5-nitro-1H-indole
询价tert-butyl N-{[3-(aminomethyl)bicyclo[1.1.1]pentan-1-yl]methyl}carbamate
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- 文献和实验
- 技术资料
- 保存条件：
Recommended Temperature controlled NMT30℃ for storage
- 英文名：
tert-butyl 4-formyl-5-methoxy-7-methyl-indole-1-carboxylate
- 供应商：
南京鼎石
- CAS号：
1481631-51-9
- 规格：
10g///25g///50g///100g///250g///500g///1kg///5kg///21880kg
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文献和实验Natural Product Chemistry in Action: The Synthesis of Melatonin Metabolites K1 and K2
melatonin, the kynurenamines N1-acetyl-N2 -formyl-5-methoxykynurenine (K1 ) and N -acetyl-5-methoxykynurenamine (K2 ). The four key synthetic transformations involve (a) conversion of 4-methoxy aniline into the tert -butyl (4-methoxyphenyl)carbamate, (b
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
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