1-Amino-2-methyl-4-bromoanthraquinone

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Names

[ CAS No. ]:
81-50-5

[ Name ]:
1-Amino-2-methyl-4-bromoanthraquinone

[Synonym ]:
Anthraquinone,1-amino-4-bromo-2-methyl
9,10-Anthracenedione, 1-amino-4-bromo-2-methyl-
1-Amino-4-brom-2-methyl-anthrachinon
1-Amino-4-bromo-2-methyl-9,10-anthraquinone
1-Amino-4-bromo-2-methylanthraquinone
EINECS 201-355-6
1-Amino-2-methyl-4-bromoanthraquinone
Anthraquinone, 1-amino-4-bromo-2-methyl-
1-amino-4-bromo-2-methyl-9,10-anthracenedione
9,10-Anthracenedione,1-amino-4-bromo-2-methyl
MFCD00001221

Chemical & Physical Properties

[ Density]:
1.6±0.1 g/cm3

[ Boiling Point ]:
526.5±50.0 °C at 760 mmHg

[ Melting Point ]:
245ºC (dec.)(lit.)

[ Molecular Formula ]:
C15H10BrNO2

[ Molecular Weight ]:
316.149

[ Flash Point ]:
272.2±30.1 °C

[ Exact Mass ]:
314.989471

[ PSA ]:
60.16000

[ LogP ]:
4.93

[ Vapour Pressure ]:
0.0±1.4 mmHg at 25°C

[ Index of Refraction ]:
1.706

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
36/37/38

[ Safety Phrases ]:
26-37/39

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2922399090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • 1-Amino-2-methyl-anthraquinone
  • Water
  • Cyclohexene
  • 2-(5-amino-2-bromo-4-methyl-benzyl)-benzoic acid
  • N-(4-bromo-2-methyl-9-oxo-9,10-dihydro-[1]anthryl)-acetamide

DownStream

  • 6-Bromo-1-carbethoxy-4-methyl-2, 7-dibenz[f,ij]isoquinoline-2,7-dione
  • 1-amino-3-methylanthracene-9,10-dione
  • 1-amino-2-methyl-4-[(4-methylphenyl)amino]anthraquinone
  • 1-ACETYL-4-METHYL-6-BROMOANTHRAPYRIDONE

Customs

[ HS Code ]: 2922399090

[ Summary ]:
2922399090 other amino-aldehydes, amino-ketones and amino-quinones, other than those containing more than one kind of oxygen function; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

Articles

Structure-activity relationships of anthraquinone derivatives derived from bromaminic acid as inhibitors of ectonucleoside triphosphate diphosphohydrolases (E-NTPDases).

Purinergic Signal. 5(1) , 91-106, (2009)

Reactive blue 2 (RB-2) had been characterized as a relatively potent ectonucleoside triphosphate diphosphohydrolase (E-NTPDase) inhibitor with some selectivity for NTPDase3. In search for the pharmaco...


More Articles

Related Compounds

  • 4-Chloro-2-Methylaniline
  • 1-amino-3-(2-methyl-4-oxo-pentan-2-yl)thiourea
  • 1-amino-1-cyclohexyl-3-(2-methyl-4-oxopentan-2-yl)thiourea
  • 1-amino-1-methyl-3-phenyl-urea
  • 1-amino-1-methyl-3-phenyl-thiourea
  • 3-amino-2-methyl-4-oxoazetidine-1-sulfonic acid
  • 1-[4-(Adamantan-1-yl)phenoxy]-3-(2,6-dimethylmorpholin-4-yl)propan-2-ol hydrochloride
  • 1-(2-(4-Chlorophenoxy)ethoxy)-3-(2,6-dimethylmorpholino)propan-2-ol hydrochloride
  • N-[(2-methylphenyl)methyl]piperidine-2-carboxamide
  • (4R)-1-Boc-4-propoxy-D-proline
  • (4S)-1-Boc-4-ethoxy-D-proline
  • 2,6-Bis[1-(2,4-dimethylphenylimino)ethyl]pyridine
  • 3-(Butan-2-YL)benzene-1,2-diol
  • 2-chloro-N-[5-(methylsulfanyl)-1,3,4-thiadiazol-2-yl]acetamide
  • N-[1-(1,3-dioxaindan-5-yl)ethyl]-2-[4-(2-phenylethenesulfonyl)piperazin-1-yl]acetamide
  • 6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-YL)pyrazin-2-amine
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