2,6-Dibromo-p-toluidine

Names

[ Name ]:
2,6-Dibromo-p-toluidine

[Synonym ]:
2,6-dibromo-4-methylphenylamine
2,6-dibromo-4-methyl Aniline
2,5-BIS(TRIFLUOROMETHYL)CHLOROBENZENE
3,5-Dibromo-4-aminotoluene
2,6-Dibromo-4-methylaniline
2,6-dibromo-4-methylbenzenamine
2,6-Dibromo-p-toluidine
Benzenamine,2,6-dibromo-4-methyl
4-methyl-2,6-dibromoaniline
EINECS 230-182-9
Benzenamine, 2,6-dibromo-4-methyl-
2,6-dibromo-4-toluidine
MFCD00007641

Chemical & Physical Properties

[ Density]:
1.9±0.1 g/cm3

[ Boiling Point ]:
283.3±35.0 °C at 760 mmHg

[ Melting Point ]:
74-76 °C(lit.)

[ Molecular Formula ]:
C₇H₇Br₂N

[ Molecular Weight ]:
264.945

[ Flash Point ]:
125.2±25.9 °C

[ Exact Mass ]:
262.894501

[ PSA ]:
26.02000

[ LogP ]:
3.87

[ Vapour Pressure ]:
0.0±0.6 mmHg at 25°C

[ Index of Refraction ]:
1.642

[ Storage condition ]:
Room temperature.

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302 + H312 + H332-H315-H319-H335

[ Precautionary Statements ]:
P261-P280-P305 + P351 + P338

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

[ Hazard Codes ]:
Xn:Harmful

[ Risk Phrases ]:
R20/21/22;R36/37/38

[ Safety Phrases ]:
S26-S37/39-S36/37/39

[ RIDADR ]:
UN 2811

[ WGK Germany ]:
3

[ Packaging Group ]:
I; II; III

[ Hazard Class ]:
6.1

[ HS Code ]:
2921430090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2921430090

[ Summary ]:
HS:2921430090 toluidines and their derivatives; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

Articles

Bimetallic phenylene-bridged Cp/amide titanium complexes and their olefin polymerization.

Dalton Trans. (40) , 4608-14, (2007)

Bimetallic dichlorotitanium complexes, {2,6-[eta(5)-2,5-Me2C5H2](2)-4-R-C6H2N-microN}{Ti(IV)Cl2}2 (, R=Me; , R=F) and 4,4'-A[{2-(eta(5)-2,3,5-Me3C5H)C6H3NC6H11-kappaN}Ti(IV)Cl2]2 (, A=CH2; , A=O; , A=...

Preparation of reagents for the sensitive spectrophotometric determination of carbaryl in environmental samples. Suresh KK, et al.

Anal. Lett. 38(4) , 697-709, (2005)

Asymmetric reactions of axially chiral amides: use of removable ortho-substituents in radical cyclizations of o-iodoacrylanilides and N-allyl-N-o-iodoacrylamides. Petit M, et al.

Tetrahedron 60(35) , 7543-52, (2005)