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CS-W001157 4
Total: USD 88.00

(E)-3-(4-Nitrophenyl)acrylic acid

  • CAS No. 882-06-4

  • Cat. No. CS-0076962
  • Purity≥98%
  • MDL No.MFCD00007381

*For research and further manufacturing use only, not for direct human use.

(E)-3-(4-Nitrophenyl)acrylic acid|CS-0076962

Structure of 882-06-4

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General Information

  • CAS No. 882-06-4
  • Cat. No. CS-0076962
  • Purity ≥98%
  • MDL No. MFCD00007381
  • Storage Sealed in dry,2-8℃
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₉H₇NO₄
  • Molecular Weight 193.16
  • Synonym(s) None
  • SMILES O=C(O)/C=C/C1=CC=C([N+]([O-])=O)C=C1

Description

6-Maleimidocaproic acid PFP ester contains a maleimide and PFP ester end group. Maleimides react with thiol groups within the pH range of 6.5 to 7.5 and form stable thioester bonds. PFP is an activated ester which can react with amine groups to form stable amide bonds.

Synthesis

  • Route1
    • null|null
      79-10-7
    • null|null
      586-78-7
    • ~94%
    • (E)-3-(4-Nitrophenyl)acrylic acid|CS-0076962
      882-06-4

    References

    • Bumagin, N. A.; Bykov, V. V.; Beletskaya, I. P. Russian Journal of Organic Chemistry, 1995 , vol. 31, # 4 p. 439 - 444 Zhurnal Organicheskoi Khimii, 1995 , vol. 31, # 4 p. 481 - 487
  • Route2
    • null|null
      636-98-6
    • null|null
      79-10-7
    • ~99%
    • (E)-3-(4-Nitrophenyl)acrylic acid|CS-0076962
      882-06-4

    References

    • Liu, Xiang; Yao, Kai; Hu, Yu-Lin; Lu, Ming Journal of Chemical Research, 2011 , vol. 35, # 12 p. 731 - 733
  • Route3

    References

    • SMITHKLINE BEECHAM CORPORATION Patent: WO2007/18941 A2, 2007 ; Location in patent: Page/Page column 93 ; WO 2007/018941 A2

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07,GHS08
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H315-H319-H335-H340
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

Quality Control

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Computational Chemistry Data

  • TPSA   80.44
  • LogP   1.6926
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   3

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