5-Pyrim­idinyl­boron­i­cacid CAS 109299-78-7

• Iden­ti­fi­ca­tion
• Prop­er­ties
• Safe­ty Data
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Iden­ti­fi­ca­tion

CAS Number

109299-78-7

Name

5-Pyrim­idinyl­boron­i­­cacid

Syn­onyms

(pyrimidin-5-yl)boronic acid

109299-78-7

[RN]
5-Pyrim­idinyl­boron­ic acid

[IUPAC name – gen­er­at­ed by ACD/​Name]
5-Pyrim­idinyl­borsäure

[Ger­man]

[IUPAC name – gen­er­at­ed by ACD/​Name]
Acide 5-pyrim­idinyl­boronique

[French]

[IUPAC name – gen­er­at­ed by ACD/​Name]
Acide pyrim­idin-5-ylboronique

[French]

Boron­ic acid, B-5-pyrimidinyl-

[IUPAC index name – gen­er­at­ed by ACD/​Name]
Pyrim­idin-5-ylboron­ic acid

Pyrim­i­­dine-5-boron­ic acid

SMILES

OB(O)c1cncnc1

Std­InChI

InChI=1S/C4H5BN2O2/c8-5(9)4-1-6-3-7-2-4/h1-3,8-9H

Std­InChIKey

HZF­PPBMK­­GYINDF-UHF­F­­FAOYSA-N

Mol­e­c­u­lar Formula

C4H5BN2O2

Mol­e­c­u­lar Weight

123.908

MDL Number

MFCD03002366

Prop­er­ties

Appear­ance

Off-white pow­der

Safe­ty Data

Sym­bol

GHS05, GHS07

Sig­nal Word

Warn­ing

Haz­ard statements

Pre­cau­tion­ary Statements

WGK Germany

3

MSDS Download

Spec­i­fi­ca­tions and Oth­er Infor­ma­tion of Our 5-Pyrim­idinyl­boron­i­­cacid CAS 109299-78-7

Iden­ti­fi­ca­tion Methods

HPLC

Puri­ty

97% min

Known Appli­ca­tion

1. Suzu­ki – Miyau­ra Cou­pling Reac­tions Wide­ly used as a boron­ic acid build­ing block in pal­la­di­um-cat­­a­lyzed cross-cou­­pling reac­tions with aryl or vinyl halides. Enables the syn­the­sis of pyrim­i­­dine-con­­tain­ing biaryl and het­eroaryl com­pounds. 2. Phar­ma­ceu­ti­cal Inter­me­di­ates Serves as a key inter­me­di­ate in the prepa­ra­tion of drug can­di­dates, espe­cial­ly kinase inhibitors, antivi­ral agents, and anti­cancer com­pounds that incor­po­rate the pyrim­i­dine motif. 3. Agro­chem­i­cal Syn­the­sis Applied in the design and syn­the­sis of het­eroaryl deriv­a­tives used in her­bi­cides, fungi­cides, and insec­ti­cides. 4. Mate­r­i­al Sci­ence Some­times employed in the devel­op­ment of func­tion­al mate­ri­als, such as con­ju­gat­ed het­eroaryl poly­mers or lig­ands for coor­di­na­tion chem­istry. 5. Med­i­c­i­nal Chem­istry Research Use­ful for struc­ture – activ­i­ty rela­tion­ship (SAR) stud­ies, intro­duc­ing pyrim­i­dine groups into mol­e­cules to mod­u­late bio­log­i­cal activ­i­ty and improve bind­ing affinity.

Gen­er­al View of Documents

Links

This prod­uct is devel­oped by our R&D com­pa­ny Cam­ing Phar­ma­ceu­ti­cal Lim­it­ed (http://​www​.cam​ing​.com/).

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