4-Iodobiphenyl

Names

[ CAS No. ]:
1591-31-7

[ Name ]:
4-Iodobiphenyl

[Synonym ]:
EINECS 216-469-1
4-Iodbiphenyl
MFCD00019028
4-iodo-1,1'-biphenyl

Chemical & Physical Properties

[ Density]:
1.6±0.1 g/cm3

[ Boiling Point ]:
322.7±21.0 °C at 760 mmHg

[ Melting Point ]:
110-114 °C

[ Molecular Formula ]:
C₁₂H₉I

[ Molecular Weight ]:
280.104

[ Flash Point ]:
145.8±11.1 °C

[ Exact Mass ]:
279.974884

[ LogP ]:
4.98

[ Vapour Pressure ]:
0.0±0.7 mmHg at 25°C

[ Index of Refraction ]:
1.641

MSDS

Safety Information

[ Symbol ]:

GHS05, GHS07, GHS09

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H302-H318-H410

[ Precautionary Statements ]:
P273-P280-P305 + P351 + P338-P501

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

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S39-S60-S61-S37/39

[ RIDADR ]:
UN 3077 9/PG 3

[ WGK Germany ]:
3

[ Packaging Group ]:
III

[ Hazard Class ]:
9

[ HS Code ]:
2903999090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

Biphenyl
4-Bromobiphenyl
4-Biphenylboronic acid
Benzyl cyanide
4-Aminobiphenyl
1,4-Diiodobenzene
benzene
4-Iodobenzenediazonium tetrafluoroborate
Phenylboronic acid

DownStream

1,1':4',1'':4'',1''':4''',1''''-Quinquephenyl
p-quaterphenyl
p-Sexiphenyl
4-Biphenylboronic acid
pnb
4-Biphenylol
4-Bromobiphenyl
3-BIPHENYL-4-YLPROP-2-YN-1-OL
1,2-Di([1,1'-biphenyl]-4-yl)ethyne
4-Biphenylcarboxylic acid

Customs

[ HS Code ]: 2903999090

[ Summary ]:
2903999090 halogenated derivatives of aromatic hydrocarbons VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%

Articles

Update on biological actions of 1alpha,25(OH)2-vitamin D3 (rapid effects) and 24R,25(OH)2-vitamin D3.

Biochem. Pharmacol. 31(10) , 1849-56, (1982)

All biologic responses to vitamin D are now known to arise as a consequence of the metabolism of this seco-steroid into its two principal biologically active metabolites 1alpha,25(OH)(2)-vitamin D(3) ...

Biodehalogenation and metabolism of 125[I]-4-iodobiphenyl.

J. Pharm. Sci. 70(5) , 546-9, (1981)

[125I]-4-Iodobiphenyl has been used as a model compound to investigate the in vivo metabolism of iodinated aromatic compounds in the rat. Material balance studies showed that 57.6% of the injected dos...