15528
Boc-Val-OH
≥99.0% (T)
别名:
(S)-2-(叔丁氧羰基氨基)-3-甲基丁酸, N-(叔丁氧羰基)-L-缬氨酸, Boc-L-缬氨酸
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关于此项目
线性分子式:
(CH3)2CHCH(COOH)NHCOOC(CH3)3
化学文摘社编号:
分子量:
217.26
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
32160406
UNSPSC Code:
12352209
EC Number:
237-307-6
MDL number:
Beilstein/REAXYS Number:
1711290
InChI key
SZXBQTSZISFIAO-ZETCQYMHSA-N
InChI
1S/C10H19NO4/c1-6(2)7(8(12)13)11-9(14)15-10(3,4)5/h6-7H,1-5H3,(H,11,14)(H,12,13)/t7-/m0/s1
SMILES string
CC(C)[C@H](NC(=O)OC(C)(C)C)C(O)=O
assay
≥99.0% (T)
form
solid
optical activity
[α]20/D −6.2±0.5°, c = 1% in acetic acid
reaction suitability
reaction type: Boc solid-phase peptide synthesis, reaction type: C-H Activation, reagent type: ligand
reaction type: Peptide Synthesis
mp
77-80 °C (lit.)
application(s)
peptide synthesis
functional group
amine, carboxylic acid
Quality Level
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存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
Ye Sheng et al.
International journal of pharmaceutics, 487(1-2), 242-249 (2015-04-19)
Amino acid and dipeptide prodrugs have been developed to examine their potential in enhancing aqueous solubility and permeability as well as to bypass P-glycoprotein (P-gp) mediated cellular efflux of prednisolone. Prodrugs have been synthesized and identified with LC/MS/MS and NMR.
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