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- AMEKO
- 中国
- AB65007-1g
- 2025年08月14日
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- 详细信息
- 文献和实验
- 技术资料
- 保存条件：
2-8℃
- 英文名：
Bis-Boc-Amino-Oxyacetic Acid
- 库存：
99
- 供应商：
联硕生物
- CAS号：
293302-31-5
- 规格：
1g
纯度：98%
保存温度：2-8℃
英文名称：Bis-Boc-Amino-Oxyacetic Acid
分子式：C12H21NO7
GONXCYWPDEIQFAZSBULKTVJHMR
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文献和实验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
Methylated Polyamines as Research Tools
resulted in corresponding di-Boc-amines, which after deprotection gave target β- and γ-MeSpd’s. To prepare α-MeSpd, the starting compound, 3-amino-1-butanol, was converted into N -Cbz-3-amino-1-butyl methanesulfonate, which alkylated putrescine
Synthesis and Probing of Membrane-bound Peptide Arrays
should be Cys(Acm) or Cys(Trt), Asp(OtBu), Glu(OtBu), His(Trt), Lys(Boc), Asn(Trt), Gln(Trt), Arg(Pmc), Ser(tBu), Thr(tBu), Trp(Boc), and Tyr(tBu). HOBt-esters of these amino acid derivatives must be prepared in NMP for use throughout in spotting reactions
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