2,6-Dichlorobenzoyl chloride

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Names

[ CAS No. ]:
4659-45-4

[ Name ]:
2,6-Dichlorobenzoyl chloride

[Synonym ]:
GVR BG FG
EINECS 225-102-4
2,6-dichloro-1-benzenecarbonyl chloride
Benzoyl chloride,2,6-dichloro
2,6-Dichlorobenzoyl chloride
MFCD00000662
Benzoyl chloride, 2,6-dichloro-
2,6-dichloro-benzoyl chloride

Chemical & Physical Properties

[ Density]:
1.5±0.1 g/cm3

[ Boiling Point ]:
260.4±20.0 °C at 760 mmHg

[ Melting Point ]:
15-17 °C

[ Molecular Formula ]:
C7H3Cl3O

[ Molecular Weight ]:
209.457

[ Flash Point ]:
107.4±22.3 °C

[ Exact Mass ]:
207.924942

[ PSA ]:
17.07000

[ LogP ]:
2.57

[ Vapour Pressure ]:
0.0±0.5 mmHg at 25°C

[ Index of Refraction ]:
1.577

[ Storage condition ]:
2-8°C

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-S36/37/39-S45

[ RIDADR ]:
UN 3265 8/PG 2

[ WGK Germany ]:
1

[ Packaging Group ]:
II

[ Hazard Class ]:
8

[ HS Code ]:
29163900

Synthetic Route

Precursor & DownStream

Precursor

  • 2,6-Dichlorobenzoic acid
  • 2,6-Dichlorobenzaldehyde

DownStream

  • 5-(2,6-dichlorophenyl)-2,4-dimethyl-1,2,4-triazole-3-thione
  • [(2,6-dichlorobenzoyl)-phenylphosphoryl]-(2,6-dichlorophenyl)methanone
  • 2,6-Difluorobenzoic acid
  • 2,6-Dichlorobenzoic acid
  • TR 14035
  • ethyl 2,6-dichlorobenzoate
  • BAM
  • 2,6-Dichlorobenzaldehyde
  • tributyl(chloro)germane
  • Ethyl 2,6-dichlorobenzoylacetate

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

Substrate activity screening (SAS): a general procedure for the preparation and screening of a fragment-based non-peptidic protease substrate library for inhibitor discovery.

Nat. Protoc. 2(2) , 424-33, (2007)

Substrate activity screening (SAS) is a fragment-based method for the rapid development of novel substrates and their conversion into non-peptidic inhibitors of Cys and Ser proteases. The method consi...

Sensitisation to dichlorobenzoyl chloride.

Contact Dermatitis 18(2) , 116-7, (1988)

An improved method for anchoring of 9-fluorenylmethoxycarbonyl-amino acids to 4-alkoxybenzyl alcohol resins. Sieber, P.

Tetrahedron Lett. 28(49) , 6147-50, (1987)


More Articles


Related Compounds

  • (E)-2,6-dichlorobenzoyl chloride oxime
  • 2,6-dichlorobenzoyl isothiocyanate
  • 2,6-dichlorobenzoyl isocyanate
  • [(2,6-dichlorobenzoyl)-phenylphosphoryl]-(2,6-dichlorophenyl)methanone
  • [(2,6-dichlorobenzoyl)-(4-propylphenyl)phosphoryl]-(2,6-dichlorophenyl)methanone
  • 3,6-DICHLORO-ORTHO-ANISICACIDCHLORIDE
  • 2-((3-(2-methoxyethyl)-4-oxo-3,4,6,7-tetrahydrothieno[3,2-d]pyrimidin-2-yl)thio)-N-(3-nitrophenyl)acetamide
  • 4-(2-((2-Isobutyl-6,8-dimethyl-5,7-dioxo-5,6,7,8-tetrahydropyrimido[4,5-d]pyrimidin-4-yl)thio)acetamido)benzamide
  • 7-butyl-1,3-dimethyl-5-((4-(trifluoromethyl)benzyl)thio)pyrimido[4,5-d]pyrimidine-2,4(1H,3H)-dione
  • 2-((1-(4-chlorophenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yl)thio)-N-(5-ethyl-1,3,4-thiadiazol-2-yl)acetamide
  • 2-((1-(3-chlorophenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yl)thio)-N-(5-methyl-1,3,4-thiadiazol-2-yl)acetamide
  • 2-((5-(1-(2-Methoxyphenyl)-5-oxopyrrolidine-3-carboxamido)-1,3,4-thiadiazol-2-yl)thio)hexanoic acid
  • N-((5-((2-((benzo[d][1,3]dioxol-5-ylmethyl)amino)-2-oxoethyl)thio)-1,3,4-oxadiazol-2-yl)methyl)benzamide
  • 4-(tert-butyl)-N-((5-((2-((furan-2-ylmethyl)amino)-2-oxoethyl)thio)-1,3,4-oxadiazol-2-yl)methyl)benzamide
  • 6-Amino-1-(4-methoxyphenyl)-2-{[2-oxo-2-(4-phenylpiperazin-1-yl)ethyl]sulfanyl}-1,4-dihydropyrimidin-4-one
  • 1-(2-ethylpiperidin-1-yl)-2-(1-(2-morpholino-2-oxoethyl)-1H-indol-3-yl)ethane-1,2-dione
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