5-BROMO-6-CHLORO-3-INDOLYL PHOSPHATE P-TOLUIDINE SALT

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Names

[ CAS No. ]:
6769-80-8

[ Name ]:
5-BROMO-6-CHLORO-3-INDOLYL PHOSPHATE P-TOLUIDINE SALT

[Synonym ]:
MAGENTA PHOSPHATE
5-BROMO-6-CHLORO-3-INDOLYL PHOSPHATEP-TO LUIDINE
MFCD00210023
5-Bromo-6-chloro-3-indolylphosphoric acid p-toluidine salt
5-BroMo-6-chloro-3-indoxyl phosphate p-toluidine s
5-BROMO-6-CHLORO-3-INDOXYL PHOSPHATE,P-TOLUIDINE SALT
BCIP RED P-TOLUIDINE SALT

Chemical & Physical Properties

[ Boiling Point ]:
580.2ºC at 760 mmHg

[ Melting Point ]:
198-200ºC

[ Molecular Formula ]:
C15H15BrClN2O4P

[ Molecular Weight ]:
433.62100

[ Flash Point ]:
304.7ºC

[ Exact Mass ]:
431.96400

[ PSA ]:
118.38000

[ LogP ]:
5.21370

MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xi

[ Safety Phrases ]:
24/25

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2933990090

Customs

[ HS Code ]: 2933990090

[ Summary ]:
2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

Premature chromosome condensation induced by caffeine, 2-aminopurine, staurosporine and sodium metavanadate in S-phase arrested HeLa cells is associated with a decrease in Chk1 phosphorylation, formation of phospho-H2AX and minor cytoskeletal rearrangements.

Histochem. Cell Biol. 135(3) , 263-80, (2011)

Here, we demonstrate that in HeLa cells, Ser317 of Chk1 undergoes phosphorylation in response to replication stress induced by hydroxyurea. We also demonstrate the existence of constitutive (interphas...


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Related Compounds

  • 5-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl) 2-methyl pyridine-2,5-dicarboxylate
  • Tert-butyl 4-[3-(aminomethyl)-2,6-dimethyl-5-(prop-2-yn-1-yl)phenyl]piperazine-1-carboxylate
  • Tert-butyl 4-[5-(aminomethyl)-2,4-dimethyl-3-(prop-2-yn-1-yl)phenyl]piperazine-1-carboxylate
  • 3-(Azidomethyl)-5-[(fluorosulfonyl)oxy]-2,6-dimethylbenzene-1-sulfonyl chloride
  • 2-(N-{[(cyanomethyl)carbamoyl]methyl}-1-(1-methyl-2-oxo-1,2,3,4-tetrahydroquinolin-6-yl)formamido)-N-methylacetamide
  • (9H-fluoren-9-yl)methyl 4-[(3-ethynyl-5-iodo-2,4-dimethylphenyl)methyl]piperazine-1-carboxylate
  • 2-[(3-{4-[(Tert-butoxy)carbonyl]piperazin-1-yl}-5-(methoxycarbonyl)-2-methylphenyl)methoxy]acetic acid
  • 2-[3-ethynyl-5-({[(9H-fluoren-9-yl)methoxy]carbonyl}(methyl)amino)-2-methylphenyl]acetic acid
  • N-(3-ethynyloxolan-3-yl)acetamide
  • 2-[5-ethynyl-3-({[(9H-fluoren-9-yl)methoxy]carbonyl}(methyl)amino)-2-methylphenyl]acetic acid
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