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1002127-60-7

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1002127-60-7 Usage

General Description

3,6-Dihydro-2H-pyran-4-boronic acid is a boronic acid derivative with the molecular formula C5H9BO3. It is a compound containing a boronic acid group attached to a 2,3-dihydropyran ring. This chemical is often used as a building block in the synthesis of pharmaceuticals and agrochemicals, and it has also been explored as a potential ligand in coordination chemistry. Boronic acids are known for their ability to form reversible covalent bonds with diols, making them useful in the development of sensors and diagnostics. Additionally, they have gained attention as potential inhibitors in medicinal chemistry, particularly in the field of cancer research. Overall, 3,6-dihydro-2H-pyran-4-boronic acid has diverse applications in the fields of organic synthesis, coordination chemistry, and drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 1002127-60-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,2,1,2 and 7 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1002127-60:
(9*1)+(8*0)+(7*0)+(6*2)+(5*1)+(4*2)+(3*7)+(2*6)+(1*0)=67
67 % 10 = 7
So 1002127-60-7 is a valid CAS Registry Number.

1002127-60-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,6-dihydro-2H-pyran-4-ylboronic acid

1.2 Other means of identification

Product number -
Other names 3,6-dihydro-2H-pyran-4-boronic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
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More Details:1002127-60-7 SDS

1002127-60-7Downstream Products

1002127-60-7Relevant articles and documents

Preparation of α-oxygenated ketones by the dioxygenation of alkenyl boronic acids

Patil, Aditi S.,Mo, Dong-Liang,Wang, Heng-Yen,Mueller, Daniel S.,Anderson, Laura L.

supporting information; experimental part, p. 7799 - 7803 (2012/09/08)

Two in two: Dioxygenation of alkenyl boronic acids has been achieved with N-hydroxyphthalimide. The two-step process involves etherification of an alkenyl boronic acid with N-hydroxyphthalimide followed by a [3,3] rearrangement. The dioxygenated product can then be hydrolyzed to form either the corresponding α-hydroxy ketone or the α-benzoyloxy ketone. Copyright

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