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Methyl 2-(chlorosulfonyl)-5-nitrobenzoate

Product Name
Methyl 2-(chlorosulfonyl)-5-nitrobenzoate
CAS No.
1039020-81-9
Chemical Name
Methyl 2-(chlorosulfonyl)-5-nitrobenzoate
Synonyms
Methyl 2-(chlorosulfonyl)-5-nitrobenzoate;2-Methoxycarbonyl-4-nitrobenzenesulfonyl chlorid;Benzoic acid, 2-(chlorosulfonyl)-5-nitro-, methyl ester
CBNumber
CB63131956
Molecular Formula
C8H6ClNO6S
Formula Weight
279.65
MOL File
1039020-81-9.mol
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Methyl 2-(chlorosulfonyl)-5-nitrobenzoate Property

Boiling point:
433.0±35.0 °C(Predicted)
Density 
1.590±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
Appearance
White to off-white Solid
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H314Causes severe skin burns and eye damage

Precautionary statements

P260Do not breathe dust/fume/gas/mist/vapours/spray.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P301+P330+P331IF SWALLOWED: Rinse mouth. Do NOT induce vomiting.

P303+P361+P353IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.

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N-Bromosuccinimide Price

TRC
Product number
B495580
Product name
Methyl2-(Chlorosulfonyl)-5-nitrobenzoate
Packaging
10mg
Price
$45
Updated
2021/12/16
TRC
Product number
B495580
Product name
Methyl2-(Chlorosulfonyl)-5-nitrobenzoate
Packaging
50mg
Price
$175
Updated
2021/12/16
AK Scientific
Product number
3680DP
Product name
Methyl2-(chlorosulfonyl)-5-nitrobenzoate
Packaging
1g
Price
$330
Updated
2021/12/16
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Methyl 2-(chlorosulfonyl)-5-nitrobenzoate Chemical Properties,Usage,Production

Synthesis

53531-45-6

1039020-81-9

The general procedure for the synthesis of methyl 2-(chlorosulfonyl)-5-nitrobenzoate from the compound (CAS:53531-45-6) was as follows: first, 5.1 g (12 mmol) of 2,2'-thio-bis(4-nitrobenzoate) obtained by extraction in step (2) was dissolved in a reaction solution containing 5.04 g (60 mmol) of 95% ammonium nitrate and 42.3 mL of TMSCl (96 mmol) in 60 mL of dichloromethane to prepare the reaction solution. The reaction solution was transferred to a closed glass tube and the reaction was stirred at 50 °C for 15 to 24 h, during which the reaction progress was monitored by TLC. After completion of the reaction, the reaction solution was cooled to room temperature and filtered. Subsequently, the filtrate was washed sequentially with 200 mL of water and 100 mL of saturated brine. The filtrate was collected, dried with anhydrous Na2SO4, concentrated overnight under reduced pressure, and distilled to remove the solvent, resulting in 2.754 g of solid product, 2-methoxycarbonyl-4-nitrobenzenesulfonyl chloride, from the filtrate.

References

[1] Patent: CN103626708, 2016, B. Location in patent: Paragraph 0064-0066

Methyl 2-(chlorosulfonyl)-5-nitrobenzoate Preparation Products And Raw materials

Raw materials

Preparation Products

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1039020-81-9, Methyl 2-(chlorosulfonyl)-5-nitrobenzoateRelated Search:


  • Methyl 2-(chlorosulfonyl)-5-nitrobenzoate
  • 2-Methoxycarbonyl-4-nitrobenzenesulfonyl chlorid
  • Benzoic acid, 2-(chlorosulfonyl)-5-nitro-, methyl ester
  • 1039020-81-9
  • C8H6ClNO6S