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isopropyl cyclopropanesulfonate

Product Name
isopropyl cyclopropanesulfonate
CAS No.
146475-51-6
Chemical Name
isopropyl cyclopropanesulfonate
Synonyms
2-propyl cyclopropanesulfonate;isopropyl cyclopropanesulfonate;1-Methylethyl cyclopropanesulfonate;Cyclopropanesulfonic acid, 1-methylethyl ester
CBNumber
CB42596118
Molecular Formula
C6H12O3S
Formula Weight
164.22
MOL File
146475-51-6.mol
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isopropyl cyclopropanesulfonate Property

storage temp. 
Sealed in dry,Store in freezer, under -20°C
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Safety

HS Code 
2904100090
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
I779110
Product name
IsopropylCyclopropanesulfonate
Packaging
500mg
Price
$155
Updated
2021/12/16
AK Scientific
Product number
1896AQ
Product name
Isopropylcyclopropanesulfonate
Packaging
1g
Price
$178.4
Updated
2021/12/16
Apolloscientific
Product number
OR950828
Product name
Isopropylcyclopropanesulfonate
Purity
95%
Packaging
1g
Price
$261
Updated
2021/12/16
Apolloscientific
Product number
OR950828
Product name
Isopropylcyclopropanesulfonate
Purity
95%
Packaging
5g
Price
$769
Updated
2021/12/16
Chemenu
Product number
CM203687
Product name
isopropylcyclopropanesulfonate
Purity
95+%
Packaging
10g
Price
$337
Updated
2021/12/16
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isopropyl cyclopropanesulfonate Chemical Properties,Usage,Production

Synthesis

139631-62-2

67-63-0

146475-51-6

Isopropanol (11 L) was slowly added to pyridine (1850 g; 1890 mL) at 20 °C with continuous stirring for 1 hour. Subsequently, the reaction system was cooled to -10 °C to 2 °C and cyclopropanesulfonyl chloride (1100 g) was added dropwise. After the dropwise addition, the reaction was kept at this temperature with continued stirring for 70 hours. Consumption of cyclopropanesulfonyl chloride was confirmed to be 85% by NMR analysis. The reaction mixture was further cooled to 0 °C and an aqueous solution (600 mL) of sodium hydroxide (312 g) was added dropwise. Upon completion of the reaction, the mixture was concentrated to dryness at 45 °C. The concentrate was diluted with ethyl acetate (2750 mL) and methyl tert-butyl ether (1375 mL), stirred for 10 minutes and filtered. To the filtrate was added heptane (1375 mL), filtered again and the filtrate was concentrated to dryness to give 1080 g of isopropyl cyclopropyl sulfonate as a red liquid in 84% yield. The structure of the product was confirmed by 1H NMR (CDCl3, 400 MHz): δ 4.86 (m, 1H), 2.83 (m, 1H), 1.33 (d, 6H), 0.98-1.10 (m, 4H).

References

[1] Patent: US2012/316149, 2012, A1. Location in patent: Page/Page column 13; 14
[2] Patent: WO2012/168884, 2012, A1. Location in patent: Page/Page column 33
[3] Patent: WO2010/145197, 2010, A1. Location in patent: Page/Page column 67-68
[4] Patent: EP3312172, 2018, A1. Location in patent: Paragraph 0399; 0400

isopropyl cyclopropanesulfonate Preparation Products And Raw materials

Raw materials

Preparation Products

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isopropyl cyclopropanesulfonate Suppliers

Jia Xing Isenchem Co.,Ltd
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Tel
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Aikon International Limited
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Henan Alpha Chemical Co., Ltd.
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146475-51-6, isopropyl cyclopropanesulfonateRelated Search:


  • isopropyl cyclopropanesulfonate
  • 2-propyl cyclopropanesulfonate
  • Cyclopropanesulfonic acid, 1-methylethyl ester
  • 1-Methylethyl cyclopropanesulfonate
  • 146475-51-6