6,6''-Dibrom-2,2':6',2''-terpyridin

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Names

[ CAS No. ]:
100366-66-3

[ Name ]:
6,6''-Dibrom-2,2':6',2''-terpyridin

[Synonym ]:
6,6''-Dibrom-2,2':6',2''-terpyridin
2,6''-dibromo-2,2':6,2''-bipyridine
6,6'-dibromo-2,2':6',2''-terpyridine
2,2':6',2''-Terpyridine, 6,6''-dibromo-
MFCD01863557
6,6''-Dibromo-2,2':6',2''-terpyridine
2",6-dibromo-2,2':6',6"-terpyridine

Chemical & Physical Properties

[ Density]:
1.7±0.1 g/cm3

[ Boiling Point ]:
473.0±40.0 °C at 760 mmHg

[ Melting Point ]:
257-263ºC(lit.)

[ Molecular Formula ]:
C15H9Br2N3

[ Molecular Weight ]:
391.060

[ Flash Point ]:
239.9±27.3 °C

[ Exact Mass ]:
388.916321

[ PSA ]:
38.67000

[ LogP ]:
3.55

[ Vapour Pressure ]:
0.0±1.1 mmHg at 25°C

[ Index of Refraction ]:
1.654

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 ]:
R36/37/38

[ Safety Phrases ]:
26-36

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2933399090

Synthetic Route

Customs

[ HS Code ]: 2933399090

[ Summary ]:
2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

A tri-copper(II) complex displaying DNA-cleaving properties and antiproliferative activity against cancer cells.

Chemistry 18(47) , 15133-41, (2012)

A new disubstituted terpyridine ligand and the corresponding tri-copper(II) complex have been prepared and characterised. The binding affinity and binding mode of this tri-copper complex (as well as t...

A Novel One-Pot Synthesis of 6,6''-Dibromo-2,2':6'2''-terpyridine. Uchida Y, et al.

ChemInform 26(50) , (1995)


More Articles


Related Compounds

  • 6,6''-DIMETHYL-[2,2':6',2''-TERPYRIDINE]-4'-CARBOXYLIC ACID ETHYL ESTER
  • 6,6''-BIS(BROMOMETHYL)-[2,2':6',2''-TERPYRIDINE]-4'-CARBOXYLIC ACID ETHYL ESTER
  • 4',6,6''-trimethyl-2,2':6',2''-terpyridine
  • 3,3,3'',3''-tetrachloro-3,3'',4,4'',5,5'',6,6''-octahydro-2,2':6',2''-terpyridine
  • 6,7,8,9-tetrahydro-pyrido[1,2,a]indole-7-carboxylic acid ethyl ester
  • 2,6-bis(6-bromopyridin-2-yl)-4-phenylpyridine
  • N-(4-Fluoro-2-(trifluoromethyl)benzyl)-5-methoxy-2-(pyridin-2-yl)pyrimidin-4-amine hydrochloride
  • 2,2'-[[4,4,9,9-Tetrakis(4-hexylphenyl)-4,9-dihydrothieno[3',2':4,5]cyclopenta[1,2-b]thieno[2'',3'':3',4']cyclopenta[1',2':4,5]thieno[2,3-d]thiophene-2,7-diyl]bis[methylidyne(5-fluoro-3-oxo-1H-indene-2,1(3H)-diylidene)]]bis[propanedinitrile]
  • Rel-2-((1R,4aS,8aR)-decahydronaphthalen-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 3-(4-((4-Fluorobenzyl)oxy)phenyl)azetidine
  • 2-((3-(5-(Di-p-tolylamino)thiophen-2-yl)benzo[c]thiophen-1-yl)methylene)malononitrile
  • 2-((4-(2,2-Bis(4-hydroxyphenyl)-1-phenylvinyl)phenyl)(thiophen-2-yl)methylene)malononitrile
  • 1-(Tetrahydro-2H-pyran-3-yl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrole
  • 2,6A-dibromohexahydro-1H-spiro[[1,2,4](epimethanetriyl)cyclobuta[cd]indene-3,2'-[1,3]dioxolan]-6(4H)-one
  • (2S,8S,14S)-17-Amino-14-(hydroxymethyl)-2,8-dimethyl-4,7,10,13,16-pentaoxo-3,6,9,12,15-pentaazaheptadecan-1-oic acid
  • 2-((4-(2,2-Bis(4-(3-bromopropoxy)phenyl)-1-phenylvinyl)phenyl)(phenyl)methylene)malononitrile
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