2,4,6-Trichlorobenzoyl chloride
Names
[ CAS No. ]:
4136-95-2
[ Name ]:
2,4,6-Trichlorobenzoyl chloride
[Synonym ]:
2,4,6-Trichlorobenzoylchloride
2,4,6-Trichlorobenzoyl chloride
MFCD00075323
Benzoyl chloride, 2,4,6-trichloro-
Chemical & Physical Properties
[ Density]:
1.6±0.1 g/cm3
[ Boiling Point ]:
284.2±35.0 °C at 760 mmHg
[ Molecular Formula ]:
C7H2Cl4O
[ Molecular Weight ]:
243.902
[ Flash Point ]:
118.5±26.5 °C
[ Exact Mass ]:
241.885971
[ PSA ]:
17.07000
[ LogP ]:
3.36
[ Vapour Pressure ]:
0.0±0.6 mmHg at 25°C
[ Index of Refraction ]:
1.590
MSDS
Safety Information
[ Symbol ]:
GHS05
[ Signal Word ]:
Danger
[ Hazard Statements ]:
H314
[ Precautionary Statements ]:
P280-P305 + P351 + P338-P310
[ Personal Protective Equipment ]:
Faceshields;full-face respirator (US);Gloves;Goggles;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter
[ Hazard Codes ]:
C:Corrosive;
[ Risk Phrases ]:
R34
[ Safety Phrases ]:
S26-S27-S28-S36/37/39-S45-S25
[ RIDADR ]:
UN 3265 8/PG 2
[ WGK Germany ]:
3
[ Packaging Group ]:
II
[ Hazard Class ]:
8
[ HS Code ]:
2916399090
Synthetic Route
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2916399090
[ Summary ]:
2916399090 other aromatic monocarboxylic acids, their anhydrides, halides, peroxides, peroxyacids and their derivatives VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%
Articles
Carbohydr. Polym. 111 , 883-91, (2014)
The present work describes a novel and efficient method of synthesis of amphiphilic hyaluronan (HA) by esterification with alkyl fatty acids. These derivatives were synthesized under mild aqueous and ...
Asymmetric total synthesis of spongistatins 1 and 2.J. Am. Chem. Soc. 124(20) , 5661-63, (2002)
The total synthesis of spongistatin 1 (1) and spongistatin 2 (2) has been achieved through an advanced-stage intermediate. The synthesis is highlighted by a highly convergent assembly of the four key ...
Synthesis of γ- and δ-lactone natural products by employing a trans-cis isomerization/lactonization strategy.Chem. Pharm. Bull. 61(4) , 464-70, (2013)
Alkaline hydrolysis of 4-hydroxy- or/and 5-hydroxy-(2E)-alkenoate followed by acid treatment gave the corresponding (2E)-alkenoic acids which were subjected to lactone formation reaction without furth...