- 询价
- 甄准
- 国外
- ZC-40828
- 2025年07月15日
企业认证
相关产品推荐更多 >
![[二甲基-2H6]-利谷隆](https://img1.dxycdn.com/2021/0422/722/0838808508190696743-14.jpg!wh200)
![[2H3]-治草醚](https://img1.dxycdn.com/2018/1115/690/3311963525975108770-14.jpg!wh200)
万千商家帮你免费找货
0 人在求购买到急需产品
- 详细信息
- 文献和实验
- 技术资料
- CAS号：
294659-72-6
- 规格：
0.1 g
风险提示：丁香通仅作为第三方平台，为商家信息发布提供平台空间。用户咨询产品时请注意保护个人信息及财产安全，合理判断，谨慎选购商品，商家和用户对交易行为负责。对于医疗器械类产品，请先查证核实企业经营资质和医疗器械产品注册证情况。
文献和实验Over the past 20 years, amino acid analysis methods based on precolumn derivatization procedures have become a popular alternative to the traditional postcolumn derivatization techniques based on ion-exchange separation of the underivatized
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
技术资料暂无技术资料 索取技术资料
