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

Click to get detail 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

  • 2-(4-{[(Tert-butoxy)carbonyl]amino}-3-methoxyphenyl)-3-methylbutanoic acid
  • 3-(4-{[(Tert-butoxy)carbonyl]amino}-2-hydroxyphenyl)-2-hydroxypropanoic acid
  • 1-(5-Bromopyridin-3-yl)-3-oxocyclobutane-1-carboxylic acid
  • 4-(5-Bromo-2-fluoropyridin-3-yl)-2-methylbutanoic acid
  • 1-[(2-Bromo-6-methoxyphenyl)methyl]cyclopropane-1-carboxylic acid
  • 2-[1-(5-Bromo-1,3-thiazol-2-yl)cyclopropyl]-2-hydroxyacetic acid
  • 2-(2-Bromo-4-nitrophenyl)-2-oxoacetic acid
  • tert-butyl N-[1-(4-methoxypiperidin-4-yl)propan-2-yl]-N-methylcarbamate
  • 5-methoxy-3-(4-methyl-1H-imidazol-5-yl)-5-oxopentanoic acid
  • tert-butyl N-[4-(2-amino-1,1-difluoropropan-2-yl)-2-methoxyphenyl]carbamate
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