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  3. (4-(tert-Butoxycarbonyl)phenyl)boronic acid

(4-(tert-Butoxycarbonyl)phenyl)boronic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

For research use only. We do not sell to patients.

(4-(tert-Butoxycarbonyl)phenyl)boronic acid Chemical Structure

(4-(tert-Butoxycarbonyl)phenyl)boronic acid Chemical Structure

CAS No. : 850568-54-6

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Based on 1 publication(s) in Google Scholar

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Description

(4-(tert-Butoxycarbonyl)phenyl)boronic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

In Vitro

Benzene boronic acid mediated the ortho specific hydroxylalkylation of phenols by aldehydes. The ability of boronic acids to reversibly bind diol functional groups has been utilized for fluorescent detection of saccharides. It can be an effective catalyst for amidation and esterification of carboxylic acids.

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Molecular Weight

222.05

Formula

C11H15BO4

CAS No.
Appearance

Solid

Color

White to off-white

SMILES

CC(C)(OC(C1=CC=C(B(O)O)C=C1)=O)C

Shipping

Room temperature in continental US; may vary elsewhere.

Storage
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
Purity & Documentation

Purity: 99.71%

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(4-(tert-Butoxycarbonyl)phenyl)boronic acid Related Classifications

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The dilution calculator equation

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This equation is commonly abbreviated as: C1V1 = C2V2

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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Product Name:
(4-(tert-Butoxycarbonyl)phenyl)boronic acid
Cat. No.:
HY-W012408
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