• Product Name2,4,6-Trichlorobenzoyl chloride
  • CasNo. 4136-95-2
  • MFC7H2Cl4O
  • MW243.904
  • Purity
  • Appearanceclear yellow liquid
  • Packing
  • Contact usInquiry

Product Details

CasNo: 4136-95-2

MF: C7H2Cl4O

Appearance: clear yellow liquid

Trustworthy Factory Supply High Purity 4136-95-2 with Competitive Price

  • Molecular Formula:C7H2Cl4O
  • Molecular Weight:243.904
  • Appearance/Colour:clear yellow liquid 
  • Vapor Pressure:0.00302mmHg at 25°C 
  • Melting Point:165-166 °C 
  • Refractive Index:n20/D 1.5754(lit.)  
  • Boiling Point:284.215 °C at 760 mmHg 
  • Flash Point:118.47 °C 
  • PSA:17.07000 
  • Density:1.608 g/cm3 
  • LogP:4.02580 

2,4,6-Trichlorobenzoyl chloride(Cas 4136-95-2) Usage

InChI:InChI=1/C7H2Cl4O/c8-3-1-4(9)6(7(11)12)5(10)2-3/h1-2H

4136-95-2 Relevant articles

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Fuson,Bertetti,Ross

, p. 4380,4382 (1932)

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Synthesis, pH dependent, plasma and enzymatic stability of bergenin prodrugs for potential use against rheumatoid arthritis

Singh, Rohit,Kumar, Vikas,Bharate, Sonali S.,Vishwakarma, Ram A.

, p. 5513 - 5521 (2017/10/06)

Bergenin is a unique C-glycoside natural...

SUBSTITUTED 1,2,5-OXADIAZOLE COMPOUNDS AND THEIR USE AS HERBICIDES

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Page/Page column 123, (2013/06/05)

The present invention relates to substit...

JANUS KINASE INHIBITOR COMPOUNDS AND METHODS

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Page/Page column 100, (2010/12/29)

The invention provides compounds of Form...

Solid-phase synthesis of new saphenamycin analogues with antimicrobial activity

Laursen, Jane B.,De Visser, Peter C.,Nielsen, Henrik K.,Jensen, Knud J.,Nielsen, John

, p. 171 - 175 (2007/10/03)

An array of 12 new saphenamycin analogue...

4136-95-2 Process route

2,4,6-trichlorobenzoic acid
50-43-1

2,4,6-trichlorobenzoic acid

2,4,6-trichlorobenzoyl chloride
4136-95-2

2,4,6-trichlorobenzoyl chloride

Conditions
Conditions Yield
With phosphorus pentachloride;
 
With phosphorus pentachloride;
 
With thionyl chloride;
 
With oxalyl dichloride; N-ethyl-N,N-diisopropylamine; N,N-dimethyl-formamide; In dichloromethane; N,N-dimethyl-formamide; at 20 ℃; for 1h;
 
With thionyl chloride; Reflux;
 
With thionyl chloride; at 70 ℃; for 2h;
 
With thionyl chloride;
 
2-bromo-6-chloro-4-methylaniline
135340-78-2

2-bromo-6-chloro-4-methylaniline

2,4,6-trichlorobenzoyl chloride
4136-95-2

2,4,6-trichlorobenzoyl chloride

Conditions
Conditions Yield
Multi-step reaction with 5 steps
1: 1.) concd. H2SO4, NaNO2 / 1.) HOAc, 15 deg C, 3 h, 2.) H2O, 35-40 deg C, 1 h
2: 40.8 percent / concd. H2SO4 / 3 h / Heating
3: 77.4 percent / concd. HCl, NaNO2, HOAc / H2O / 1.) 5 deg C, 30 min, 2.) 85 deg C, 1 h
4: SOCl2, DMF / 3 h / Heating
5: SOCl2, DMF / 3 h / Heating
With hydrogenchloride; thionyl chloride; sulfuric acid; acetic acid; N,N-dimethyl-formamide; sodium nitrite; In water;
 

4136-95-2 Upstream products

  • 50-43-1
    50-43-1

    2,4,6-trichlorobenzoic acid

  • 135365-02-5
    135365-02-5

    2-Bromo-6-chloro-4-methyl-benzoyl chloride

  • 135340-78-2
    135340-78-2

    2-bromo-6-chloro-4-methylaniline

  • 135340-79-3
    135340-79-3

    2-bromo-6-chloro-4-methylbenzonitrile

4136-95-2 Downstream products

  • 52120-00-0
    52120-00-0

    1-(2,4,6-trichloro-phenyl)-ethanone

  • 65305-79-5
    65305-79-5

    1,3-bis-(2,4,6-trichloro-phenyl)-propane-1,3-dione

  • 25187-07-9
    25187-07-9

    2-benzoyl-1,3,5-trichlorobenzene

  • 137601-32-2
    137601-32-2

    (2Z)-2-methyl-2-butenoic 2,4,6-trichlorobenzoic anhydride

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