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305129-54-8

3-(phenylamino)phenoxyacetic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 305129-54-8 Structure

  • Basic information

    1. Product Name: 3-(phenylamino)phenoxyacetic acid
    2. Synonyms:
    3. CAS NO:305129-54-8
    4. Molecular Formula:
    5. Molecular Weight: 243.262
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 305129-54-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3-(phenylamino)phenoxyacetic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(phenylamino)phenoxyacetic acid(305129-54-8)
    11. EPA Substance Registry System: 3-(phenylamino)phenoxyacetic acid(305129-54-8)

  • 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: 305129-54-8(Hazardous Substances Data)

305129-54-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 305129-54-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,5,1,2 and 9 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 305129-54:
(8*3)+(7*0)+(6*5)+(5*1)+(4*2)+(3*9)+(2*5)+(1*4)=108
108 % 10 = 8
So 305129-54-8 is a valid CAS Registry Number.

305129-54-8Downstream Products

305129-54-8Relevant articles and documents

Structure-activity relationship of orally potent tripeptide-based HIV protease inhibitors containing hydroxymethylcarbonyl isostere

Mimoto, Tsutomu,Hattori, Naoko,Takaku, Haruo,Kisanuki, Sumitsugu,Fukazawa, Tominaga,Terashima, Keisuke,Kato, Ryohei,Nojima, Satoshi,Misawa, Satoru,Ueno, Takamasa,Imai, Junya,Enomoto, Hiroshi,Tanaka, Shigeki,Sakikawa, Hiroshi,Shintani, Makoto,Hayashi, Hideya,Kiso, Yoshiaki

, p. 1310 - 1326 (2007/10/03)

We designed and synthesized a new class of peptidomimetic human immunodeficiency virus protease inhibitors containing a unique unnatural amino acid, allophenylnorstatine [Apns; (2S,3S)-3-amino-2-hydroxy-4-phenylbutyric acid], with a hydroxymethylcarbonyl isostere as the active moiety. From a structure-activity relationship study of HIV-1 protease inhibition, enzyme selectivity for other aspartyl proteases, the antiviral activity and pharmacokinetics in rats, 24c (KNI-227) and 24d (KNI-272, our first clinical candidate) were found to be selective and orally potent HIV protease inhibitors. Moreover, an improvement of the pharmacokinetic features of KNI-272 provided two long-lasting and highly bioavailable compounds (24g: JE-2178,h: JE-2179).

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