ZM 336372

Suppliers

Names

[ CAS No. ]:
208260-29-1

[ Name ]:
ZM 336372

[Synonym ]:
3-(Dimethylamino)-N-[3-[(4-hydroxybenzoyl)amino]-4-methylphenyl]-benzamide
Benzamide, 3-(dimethylamino)-N-[3-[(4-hydroxybenzoyl)amino]-4-methylphenyl]-
Benzamide (3-(dimethylamino)-N-[3-[(4-hydroxybenzoyl)amino]-4-methylphenyl]
N-(5-(3-dimethylaminobenzamido)-2-methylphenyl)-4-hydroxybenzamide
3-(Dimethylamino)-N-{3-[(4-hydroxybenzoyl)amino]-4-methylphenyl}benzamide
ZM 336372

Chemical & Physical Properties

[ Density]:
1.3±0.1 g/cm3

[ Boiling Point ]:
484.4±45.0 °C at 760 mmHg

[ Molecular Formula ]:
C23H23N3O3

[ Molecular Weight ]:
389.447

[ Flash Point ]:
246.8±28.7 °C

[ Exact Mass ]:
389.173950

[ PSA ]:
81.67000

[ LogP ]:
3.98

[ Appearance of Characters ]:
white to beige

[ Vapour Pressure ]:
0.0±1.3 mmHg at 25°C

[ Index of Refraction ]:
1.704

[ Storage condition ]:
-20°C

[ Water Solubility ]:
DMSO: >5mg/mL (warmed)

MSDS

Click to get detail MSDS

Safety Information

[ Hazard Codes ]:
Xi

[ RIDADR ]:
NONH for all modes of transport

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • 3-(Dimethylamino)benzoic acid
  • 3-DIMETHYLAMINOBENZOYL CHLORIDE

DownStream

Articles

Activation of protein kinase A (PKA) by 8-Cl-cAMP as a novel approach for antileukaemic therapy.

Br. J. Cancer 91 , 186-92, (2004)

Activation of PKA by cAMP agonists, such as 8-Cl-cAMP activation, selectively causes rapid apoptosis in v-abl transformed fibroblasts by inhibiting the Raf-1 kinase. Here we investigated whether 8-Cl-...


More Articles

Related Compounds

  • ZM 449829
  • ZM-447439
  • zm 244085
  • ZM 226600
  • ZM 306416
  • ZM 241385
  • 5-(3-cyclopropyl-1-methyl-1H-pyrazol-4-yl)-1,3,4-thiadiazol-2-amine
  • 3-Methylcyclohexyl chloroformate
  • 1-(2-Chlorobenzyl)-3-(difluoromethyl)-1H-pyrazole-4-carboxylic acid
  • N-ethyl-2-(4-methanesulfonyl-phenyl)-N-piperidin-4-yl-acetamide
  • 1-Ethyl-3-iodopyrazole-4-sulfonyl chloride
  • 5-Chloro-1-(4-fluorophenyl)indol-3-carbaldehyde
  • 5-(4-chloro-1-ethyl-1H-pyrazol-5-yl)-1,3,4-thiadiazol-2-amine
  • 3-Formyl-1-(propan-2-yl)-1H-indole-2-carboxylic acid
  • 5-[4-chloro-1-(propan-2-yl)-1H-pyrazol-5-yl]-1,3,4-thiadiazol-2-amine
  • 2-((Difluoromethyl)thio)benzaldehyde
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