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98008-66-3

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98008-66-3 Usage

General Description

4-((Benzyloxycarbonyl)(methyl)amino)butanoic acid, also known as Boc-amino butanoic acid, is a chemical compound that consists of a butanoic acid backbone with a benzyloxycarbonyl (Boc) protecting group attached to the amino group. The Boc group serves as a protecting group to prevent undesired reactions during chemical synthesis. 4-((benzyloxycarbonyl)(methyl)amino)butanoic acid is commonly used in peptide synthesis as a building block for creating peptides and proteins. It is typically synthesized through standard organic chemistry methods and can be used in a variety of research and industrial applications for the production of bioactive compounds and pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 98008-66-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,0,0 and 8 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 98008-66:
(7*9)+(6*8)+(5*0)+(4*0)+(3*8)+(2*6)+(1*6)=153
153 % 10 = 3
So 98008-66-3 is a valid CAS Registry Number.

98008-66-3Relevant articles and documents

HETEROBIFUNCTIONAL MOLECULES AS TEAD INHIBITORS

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Paragraph 0508-0509, (2021/09/11)

The invention relates to compounds and methods of using said compounds, as well as pharmaceutical compositions containing such compounds, for treating diseases and conditions mediated by TEAD, such as cancer.

MULTIFUNCTIONAL RADICAL QUENCHERS

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Page/Page column 51-52, (2014/05/07)

The invention provides a compound of formula (I): [insert formula (I)] wherein X, Y, and R1-R4 have any of the values defined in the specification, and salts thereof, as well as compositions comprising the compounds or salts. The compounds are useful for treating diseases associated with impaired mitochondrial function in an animal.

Synthesis and evaluation of α,α′-disubstituted phenylacetate derivatives for T-type calcium channel blockers

Lee, Hyung Kook,Lee, Yun Suk,Roh, Eun Joo,Rhim, Hyewhon,Lee, Jae Yeol,Shin, Kye Jung

scheme or table, p. 4424 - 4427 (2009/04/06)

We have synthesized and evaluated α,α′-disubstituted phenylacetate derivatives that were designed as T-type calcium channel blockers. Among them, compound 10e (IC50 = 8.17 ± 0.48 nM) showed the most potent T-type calcium current blocking activity and higher potency than Mibefradil (IC50 = 1.34 ± 0.49 μM). The PK profile and subtype selectivity over L-type calcium channel were satisfied for further animal assay using disease model.

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