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3-Allylaminocarbonylphenylboronic acid
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3-Allylaminocarbonylphenylboronic acid

CAS: 850567-29-2

Ref. 3D-FA160709

1gDiscontinued
2gDiscontinued
100mgDiscontinued
250mgDiscontinued
500mgDiscontinued

Discontinued product. For inquiries about similar products, please fill out our form or email us at .


Product Information

Name:
3-Allylaminocarbonylphenylboronic acid
Synonyms:
  • Boronic acid, B-[3-[(2-propen-1-ylamino)carbonyl]phenyl]-
  • B-[3-[(2-Propen-1-ylamino)carbonyl]phenyl]boronic acid
  • (3-(Allylcarbamoyl)phenyl)boronicacid
  • Boronic acid, [3-[(2-propenylamino)carbonyl]phenyl]-
Description:

3-Allylaminocarbonylphenylboronic acid is an intermediate used in the synthesis of nucleic acids. It is a boronic acid that can be prepared from 3-bromo-4-chlorobenzoyl chloride and phenylboronic acid. The compound is readily hydrolyzed by water to produce a nucleic acid and hydrogen borate. The compound has been shown to unblock phosphotriesters, which are intermediates for the synthesis of nucleic acids, by hydrolysis. 3-Allylaminocarbonylphenylboronic acid has also been shown to be an effective reagent for the preparation of ammonolysis products, such as amines and amino alcohols. In addition, this compound has been shown to have fluoride ion as one of its reactive groups, which can be used to synthesize fluorinated derivatives of nucleic acids with high selectivity.

Notice:
Our products are intended for lab use only. For any other use, please contact us.
Brand:
Biosynth
Long term storage:
Notes:

Chemical properties

Molecular weight:
205.02 g/mol
Formula:
C10H12BNO3
Purity:
Min. 95%
InChI:
InChI=1S/C10H12BNO3/c1-2-6-12-10(13)8-4-3-5-9(7-8)11(14)15/h2-5,7,14-15H,1,6H2,(H,12,13)
InChI key:
InChIKey=BGDGMVTUXWBLLR-UHFFFAOYSA-N
SMILES:
C=CCNC(=O)c1cccc(B(O)O)c1
MDL:
Melting point:
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EINECS:
Merck:
HS code:

Hazard Info

UN Number:
EQ:
Class:
H Statements:
P Statements:
Forbidden to fly:
Hazard Info:
Packing Group:
LQ:

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