15528
Boc-Val-OH
≥99.0% (T)
동의어(들):
(S)-2-(Boc-amino)-3-methylbutyric acid, N-(tert-Butoxycarbonyl)-L-valine, Boc-L-valine
로그인조직 및 계약 가격 보기
모든 사진(1)
About This Item
Linear Formula:
(CH3)2CHCH(COOH)NHCOOC(CH3)3
CAS Number:
Molecular Weight:
217.26
Beilstein:
1711290
EC Number:
MDL number:
UNSPSC 코드:
12352209
eCl@ss:
32160406
PubChem Substance ID:
NACRES:
NA.22
추천 제품
Quality Level
분석
≥99.0% (T)
양식
solid
광학 활성
[α]20/D −6.2±0.5°, c = 1% in acetic acid
반응 적합성
reaction type: Boc solid-phase peptide synthesis
reaction type: C-H Activation
reagent type: ligand
reaction type: Peptide Synthesis
mp
77-80 °C (lit.)
응용 분야
peptide synthesis
작용기
amine
carboxylic acid
SMILES string
CC(C)[C@H](NC(=O)OC(C)(C)C)C(O)=O
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
InChI key
SZXBQTSZISFIAO-ZETCQYMHSA-N
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Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Gloves, type N95 (US)
이미 열람한 고객
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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