60285-85-0

Basic information

• Product Name: 4-amino-6-(trichlorovinyl)benzene-1,3-disulphonyl dichloride
• Synonyms: 4-amino-6-(trichlorovinyl)benzene-1,3-disulphonyl dichloride;4-Amino-6-(trichloroethenyl)-1,3-benzenedisulfonic acid dichloride;Einecs 262-146-3;4-Amino-6-(trichlorovinyl)benzene-1,3-disulfonyl dichloride
• CAS NO: 60285-85-0
• Molecular Formula: C₈H₄Cl₅NO₄S₂
• Molecular Weight: 419.51666
• EINECS: 262-146-3
• Mol File: 60285-85-0.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 545.7°C at 760 mmHg
• Flash Point: 283.8°C
• Appearance: /
• Density: 1.849g/cm³
• Vapor Pressure: 5.79E-12mmHg at 25°C
• Refractive Index: 1.631
• CAS DataBase Reference: 4-amino-6-(trichlorovinyl)benzene-1,3-disulphonyl dichloride(CAS DataBase Reference)
• NIST Chemistry Reference: 4-amino-6-(trichlorovinyl)benzene-1,3-disulphonyl dichloride(60285-85-0)
• EPA Substance Registry System: 4-amino-6-(trichlorovinyl)benzene-1,3-disulphonyl dichloride(60285-85-0)

Safety Data

• Hazardous Substances Data: 60285-85-0(Hazardous Substances Data)

Usage

InChI:InChI=1/C8H4Cl5NO4S2/c9-7(8(10)11)3-1-4(14)6(20(13,17)18)2-5(3)19(12,15)16/h1-2H,14H2

Upstream product

• 63630-19-3 2-Nitro-4-(trichlorethenyl)benzoesulfonsaeureamid 
• 63630-18-2 4(trichloroethenyl) o-nitroaniline 
• 713-33-7 (m-nitrophenyl)trichloroethylene 
• 54619-63-5 α-trichloromethyl-(3-nitrophenyl)carbinol 
• 99-61-6 3-nitro-benzaldehyde 
• 63630-20-6 2-Amino-4-(trichlorethenyl)benzolsulfonamid 
• 710-72-5 3-pentachloroethyl-aniline 
• 63630-17-1 4-(Trichlorethenyl)anilin 
• 704-22-3 2-(3-aminophenyl)-1,1,2-trichloroethylene 
• 700-60-7 trichlorovinylbenzene 
• 60200-06-8 4-amino-6-trichlorovinyl-1,3-benzenedisulfonamide 
• 721-24-4 1-pentachloroethyl-3-nitro-benzene 
• 4714-36-7 1-nitro-4-(1,2,2-trichlorovinyl)benzene 

Downstream Products

• 60200-06-8 4-amino-6-trichlorovinyl-1,3-benzenedisulfonamide 

Relevant articles and documents

A method for preparing chlorine Shu Long

The invention discloses a preparation method of clorsulon. The preparation method comprises the steps: carrying out condensation on m-nitrobenzaldehyde with chloroform at a low temperature, then chloridizing, and carrying out elimination, hydrazine hydrate reduction, chlorosulfuric acid sulphonation and ammonification to obtain clorsulon. The use of benzene with relatively high toxicity is avoided, the use of chlorine with relatively large dangerousness is also avoided, the reduction reaction adopts more environmentally-friendly hydrazine hydrate, hydrazine hydrate reduction has less solid waste than iron powder reduction, an excellent catalyst ferric trichloride and an activated carbon carrier are selected, a by-product nitrogen gas has a good protective effect on the product, the product quality is high, the yield is equivalent to the yield reported in literature, the process is simplified, reaction conditions are mild, and the preparation method is environmentally friendly and has good industrial application prospects.