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3-(4-FLUORO-3-NITROPHENYL)PROPIONIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 160877-40-7 Structure
  • Basic information

    1. Product Name: 3-(4-FLUORO-3-NITROPHENYL)PROPIONIC ACID
    2. Synonyms: 3-(4-FLUORO-3-NITROPHENYL)PROPIONIC ACID;3-(4-Fluoro-3-nitrophenyl)propanoic acid
    3. CAS NO:160877-40-7
    4. Molecular Formula: C9H8FNO4
    5. Molecular Weight: 213.1625232
    6. EINECS: -0
    7. Product Categories: N/A
    8. Mol File: 160877-40-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3-(4-FLUORO-3-NITROPHENYL)PROPIONIC ACID(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(4-FLUORO-3-NITROPHENYL)PROPIONIC ACID(160877-40-7)
    11. EPA Substance Registry System: 3-(4-FLUORO-3-NITROPHENYL)PROPIONIC ACID(160877-40-7)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 160877-40-7(Hazardous Substances Data)

160877-40-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 160877-40-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,8,7 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 160877-40:
(8*1)+(7*6)+(6*0)+(5*8)+(4*7)+(3*7)+(2*4)+(1*0)=147
147 % 10 = 7
So 160877-40-7 is a valid CAS Registry Number.

160877-40-7Downstream Products

160877-40-7Relevant articles and documents

Benzylbenzimidazolyl derivatives

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, (2008/06/13)

Novel benzyl-benzimidazolyl derivatives as inhibitors of tyrosine kinases, particularly TIE-2, VEGFR, PDGFR, FGFR and/or FLT/KDR, for the treatment of tumors, according to formula (I), wherein the radicals R1, R2, r and s are defined according to Claim (1).

Simplified cyclic analogues of bastadin-5. Structure-activity relationships for modulation of the RyR1/FKBP12 Ca2+ channel complex

Masuno, Makoto N.,Pessah, Isaac N.,Olmstead, Marilyn M.,Molinski, Tadeusz F.

, p. 4497 - 4511 (2007/10/03)

Bastadin-5, a brominated macrodilactam from the marine sponge Ianthella basta, enhances release of Ca2+ from stores within the sarcoplasmic reticulum (SR) of muscle and nonmuscle cells by modulating RyR1/FKBP12 complex. Analogues of bastadin-5

BENZYL-BENZIMIDAZOLYL DERIVATIVES

-

Page/Page column 53, (2010/02/11)

Novel benzyl-benzimidazolyl derivatives as inhibitors of tyrosine kinases, particularly TIE-2, VEGFR, PDGFR, FGFR and/or FLT/KDR, for the treatment of tumors, according to formula (I), wherein the radicals R1, R2, r and s are defined according to Claim (1).

A unified strategy toward the synthesis of acerogenin-type macrocycles: Total syntheses of acerogenins A, B, C, and L and aceroside IV

Islas Gonzalez, Gabriela,Zhu, Jieping

, p. 914 - 924 (2007/10/03)

A general strategy for the synthesis of acerogenin-type diarylheptanoids containing an endocyclic biaryl ether bond has been developed, and convergent total syntheses of acerogenin A, B, C, and L and aceroside IV have been accomplished. Cycloetherificatio

SNAr-Based Macrocyclization: An Application to the Synthesis of Vancomycin Family Models

Beugelmans, Rene,Singh, Girij Pal,Bois-Choussy, Michele,Chastanet, Jacqueline,Zhu, Jieping

, p. 5535 - 5542 (2007/10/02)

The first examples of macrocyclization using the intramolecular SNAr reaction are reported.The method has allowed the efficient preparation of the elusive 16-membered macrocyclic COD and DOE rings related to vancomycin.The mild conditions used allow the incorporation of very racemization-prone amino acids, such as p-methoxyphenylglycine, into the peptide chain.After serving as an activator, the nitro group ortho to the diaryl ether linkage is converted either into a chlorine or a hydrogen atom, thus achieving the substitution pattern found in the vancomycin family of glycopeptides.When compound 20 was submitted to the same macrocyclization conditions, two atropisomers 21 and 22 were isolated and characterized.

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