Methyl L - ecoleucinate hydrochloride ans 18598-74-8

Methyl L - ecoleucinate hydrochloride ans 18598-74-8
Khoom Taw qhia:
Catalog tsis muaj.: SS130431
CAS TSIS MUAJ.: 18598-74-8
Assay: 99% min
Khoom npe: methyl l - ecoleucinate hydrochloride
Molecular cov mis: c7h15no2.hcl
Molecular hnyav: 181.66
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Kev tsis
Hauj lwm lawm

Hangzhou Lep Chem Co., Ltd. yog ib qho ntawm cov neeg tsim khoom lag luam me me thiab cov muag khoom ntawm methyl l {2} are cas 18598-74-8 nyob rau hauv Suav teb. Txais tos rau kev lag luam wholesale kev cai ua cov tshuaj lom neeg cov khoom lag luam ntawm cov nqi sib tw los ntawm peb lub hoobkas. Rau cov khoom lag luam pheej yig tshaj, tiv tauj peb tam sim no.

 

Cov lus qhia

 

Zog: Dawb rau tawm - dawb microcrystalline hmoov
Kev sib hloov tshwj xeeb (20 / d) (c =2, h2o): +27℃± 5 degree
Mp: 98-100 degree
Poob rau ziab: 1% Max
Assay: 99% min

 

 

 

Cov Ntawv Thov

 

Methyl l - ecoleucinate hydrochloride yog feem ntau siv nyob rau hauvPeptide synthesis thiab cov chaw tshawb fawbraws li kev tiv thaiv amino acid derivative. Nws pabcuam ua lub tsev tsim rau kev tsim kho ntawm cov kev tsim kho, trunceptides, thiab ntau dua cov peptide peptide ua ntu zus yog qhov tseem ceeb rau kev ua haujlwm roj ntsha. Cov compound kuj tseem ua haujlwm hauvKev Siv Tshuaj Kho Mob TshuajTxhawm rau npaj chiral intermediates rau synthesis ntawm cov tshuaj, enzyme inhibitors, thiab bioactive me me molecules. Ntxiv rau, nws yog siv nyob rau hauvCombinatorial Chemistry thiab Asymmetric synthesis, muab ib qho chaw nyob rau lwm yam rau kev tsim cov tsev qiv ntawv ntawm enantiomerically ntshiab teb. Nws cov dej - soluble hydrochloride fydroling, solubility, thiab cov tshuaj tiv thaiv kev ua haujlwm hauv ob lub a a organic.

 

Cov txiaj ntsig

 

Cov txiaj ntsig ntawm methyl l - ineoleucinate hydrochloride suav nrog nwsSiab coleochemical purity, reactivity, thiab solubilityCov. Qhov txhais l - Confriguration kom ntseeg tau tias poob los yog molecules khaws cov khoom siv roj ntsha thiab kev ntseeg siab. Nws daim ntawv me me tso cai rau kev tswj hwm hauv Peptide Couplings thiab tiv thaiv cov carboxyl pawg los ntawm undesired sab kev tawm tsam. Lub tshuab hydrochloride txhim kho kev ruaj khov thiab dej solubility, saib xyuas nws siv hauv a aqueous lossis cov kuab tshuaj sib xyaw. Cov khoom no ua rau nws muaj kev ntseeg tau hauv nruab nrab rau kev tsim cov khoom siv chiorrating, peptide siv yeeb tshuaj, thiab enantiomerically ntshiab. Ib qho ntxiv, nws yog sib xws nrog ntau yam ntawm cov khoom hluavtaws, nce versatility hauv kev kuaj thiab kev lag luam {6} teev cov ntawv thov.

 

Tag

 

Hauv cov ntsiab lus, methyl l - ecoleucinate hydrochloride yog ib chairal amino aciding synthesis, tshuaj lom neeg tshuaj lom neeg muag tshuaj synthesis. Nws cov kev tiv thaiv kev ua yeeb yam, tshuaj tiv thaiv ester, thiab dej {2} Soluble hydrochloride peptides thiab chiral intermediates. Nrog nws cov kev cuam tshuam, ruaj khov, thiab versatility, methyl l {} {4 4} {4 4} {4 4} {4 4} {4 4} {4 4 4} {

 

 

Cim npe nrov: methyl l - ecoleucinate hydrochloride}}}}}-

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