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Merck

15528

Sigma-Aldrich

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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About This Item

线性分子式:
(CH3)2CHCH(COOH)NHCOOC(CH3)3
CAS号:
分子量:
217.26
Beilstein:
1711290
EC號碼:
MDL號碼:
分類程式碼代碼:
12352209
eCl@ss:
32160406
PubChem物質ID:
NACRES:
NA.22

化驗

≥99.0% (T)

形狀

solid

光學活性

[α]20/D −6.2±0.5°, c = 1% in acetic acid

反應適用性

reaction type: Boc solid-phase peptide synthesis
reaction type: C-H Activation
reagent type: ligand
reaction type: Peptide Synthesis

mp

77-80 °C (lit.)

應用

peptide synthesis

官能基

amine
carboxylic acid

SMILES 字串

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 密鑰

SZXBQTSZISFIAO-ZETCQYMHSA-N

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儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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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With a growing peptide drug market the fast, reliable and uncomplicated synthesis of peptides is of paramount importance.

With a growing peptide drug market the fast, reliable and uncomplicated synthesis of peptides is of paramount importance.

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