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Detail of "77877-19-1"

  • CAS Number:
  • 77877-19-1
  • Name:
  • 2-Oxazolidinone,4-(1-methylethyl)-3-(1-oxopropyl)-, (4S)-

  • Superlist Name:
  • (S)-(+)-4-Isopropyl-3-propionyl-2-oxazolidinone
  • Molecular Structure:
  • Formula:
  • C9H15 N O3
  • Molecular Weight:
  • 185.22
  • Synonyms:
  • 2-Oxazolidinone,4-(1-methylethyl)-3-(1-oxopropyl)-, (S)-;(4S)-4-Isopropyl-3-propionyloxazolidin-2-one;(S)-4-Isopropyl-3-propanoyl-2-oxazolidinone;(S)-4-Isopropyl-3-propionyl-2-oxazolidinone
  • Density:
  • 1.094
  • Boiling Point:
  • 102-106 ºC (0.75 mmHg)
  • Flash Point:
  • >110 ºC
  • Hazard Symbols:
  • Safety:
  • S23;S24/25 Details

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CAS No.77877-19-1 (S)-(+)-4-Isopropyl-3-propionyl-2-oxazolidinone

Assay:98%

Supplier:Hangzhou Dayangchem Co., Ltd. [ China (Mainland)]

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CAS No.77877-19-1 (S)-(+)-4-Isopropyl-3-propionyl-2-oxazolidinone

1g;10g;50g;100g;500g 98%,99%ee(HPLC)

Supplier:Daicel Chiral Technologies (China)CO.,LTD [ China (Mainland)]

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CAS No.77877-19-1 (S)-(+)-4-Isopropyl-3-propionyl-2-oxazolidinone

(S)-4-Isopropyl-3-proPSonyl-2-oxazolidinone

Supplier:Kingos Chemical
Hangzhou Lohas Biotech Co., Ltd. [ China (Mainland)]

660Integral
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Tel:13429669695

Address:Room 606,Xihu Mansion,202 Wen Er Road

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CAS No.77877-19-1 (S)-(+)-4-Isopropyl-3-propionyl-2-oxazolidinone

Supplier:Achemo Sientific cooperation [ Hong Kong]

600Integral
600

Tel:00852-39711547

Address:38 Plaza,38 Shantung street,MongKoK,kowloon,Hongkong

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Reference

The chemistry of spiroacetals
The chemistry of spiroacetals. An enantiospecific synthesis of the spiroacetal moiety of milbemycins a7 and a8. Baker, Raymond; Swain, Christopher J.; Head, John C. (Dep. Chem., Univ. Southampton, Southampton SO9 5NH, UK). J. Chem. Soc., Chem.Several substances with their cas registry numbers 77877-19-1 and 70411-34-6 may be metioned in this study. Commun., (11), 874-6 (English) 1986. CODEN: JCCCAT. ISSN: 0022-4936. DOCUMENT TYPE: Journal CA Section: 26 (Biomolecules and Their Synthetic Analogs) Section cross-reference(s): 22 The title spiroacetal I was stereospecifically prepd. in 12 steps from (Z)-EtCH:CHCH2OH and lactone II. The key step was acid hydrolysis of the epoxide III with HClO4 to give the diaxial diol IV, exclusively. .
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