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4-(Dimethylcarbamoyl)phenylboronic acid_Molecular_structure_CAS_405520-68-5)
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4-(Dimethylcarbamoyl)phenylboronic acid

Catalog No. 715492 Name Sigma Aldrich
CAS Number 405520-68-5 Website http://www.sigmaaldrich.com
M. F. C9H12BNO3 Telephone 1-800-521-8956
M. W. 193.00748 Fax
Purity ≥94% Email
Storage Chembase ID: 64307

SYNONYMS

Title
4-(N,N-二甲氨基甲酰基)苯硼酸
IUPAC name
[4-(dimethylcarbamoyl)phenyl]boronic acid
IUPAC Traditional name
4-(dimethylcarbamoyl)phenylboronic acid
Synonyms
4-(Dimethylcarbamoyl)benzeneboronic acid
(4-(Dimethylaminocarbonyl)phenyl)boronic acid
4-(N,N-二甲基甲酰氨)苯基硼酸
4-Dimethylcarbamoylphenylboronic acid
[4-(N,N-Dimethylaminocarbonyl)phenyl]boronic acid
[4-(N,N-Dimethylcarbamoyl)phenyl]boronic acid
4-(N,N-Dimethylaminocarbonyl)phenylboronic acid

DATABASE IDS

MDL Number MFCD02258943
CAS Number 405520-68-5

PROPERTIES

Empirical Formula (Hill Notation) C9H12BNO3
Purity ≥94%
Melting Point 141-145 °C
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H315-H319-H335
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
GHS Precautionary statements P261-P305 + P351 + P338
Risk Statements 36/37/38
Safety Statements 26-36/37/39
Storage Temperature 2-8°C
German water hazard class 1

DETAILS

Description (English)
General description
May contain varying amounts of anhydride
Packaging
1 g in glass bottle
Application
Reactant for preparation of:
• Selective glucocorticoid receptor agonists1
• (thienopyridine)carboxamides as checkpoint 1 kinase (CHK1) inhibitors2
• [(pyrrolo[2,3-b]pyridinyl)methylene]hydroxybenzofuranones as ATP-competitive inhibitors of the mammalian target of rapamycin3
• Pyrrolopyridines as inhibitors of insulin-like growth factor-1 receptor tyrosine kinase4Reactant for:
• Copper-mediated N-arylation of quinazolinediones5
Description (简体中文)
General description
可含有不定量的酸酐
包装
1 g in glass bottle
Application
Reactant for preparation of:
• Selective glucocorticoid receptor agonists1
• (thienopyridine)carboxamides as checkpoint 1 kinase (CHK1) inhibitors2
• [(pyrrolo[2,3-b]pyridinyl)methylene]hydroxybenzofuranones as ATP-competitive inhibitors of the mammalian target of rapamycin3
• Pyrrolopyridines as inhibitors of insulin-like growth factor-1 receptor tyrosine kinase4Reactant for:
• Copper-mediated N-arylation of quinazolinediones5

REFERENCES