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t-butyl 3-(2-allyloxycarbonylethyl)-4-methyl-5-({4-methyl-5-oxo-3-[2-(p-tolylthio)ethyl]-1H-pyrrol-2(5H)-ylidene}methyl)-1H-pyrrole-2-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • t-butyl 3-(2-allyloxycarbonylethyl)-4-methyl-5-({4-methyl-5-oxo-3-[2-(p-tolylthio)ethyl]-1H-pyrrol-2(5H)-ylidene}methyl)-1H-pyrrole-2-carboxylate

    Cas No: 242127-03-3

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  • t-butyl 3-(2-allyloxycarbonylethyl)-4-methyl-5-({4-methyl-5-oxo-3-[2-(p-tolylthio)ethyl]-1H-pyrrol-2(5H)-ylidene}methyl)-1H-pyrrole-2-carboxylate

    Cas No: 242127-03-3

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  • 242127-03-3 Structure
  • Basic information

    1. Product Name: t-butyl 3-(2-allyloxycarbonylethyl)-4-methyl-5-({4-methyl-5-oxo-3-[2-(p-tolylthio)ethyl]-1H-pyrrol-2(5H)-ylidene}methyl)-1H-pyrrole-2-carboxylate
    2. Synonyms: t-butyl 3-(2-allyloxycarbonylethyl)-4-methyl-5-({4-methyl-5-oxo-3-[2-(p-tolylthio)ethyl]-1H-pyrrol-2(5H)-ylidene}methyl)-1H-pyrrole-2-carboxylate
    3. CAS NO:242127-03-3
    4. Molecular Formula:
    5. Molecular Weight: 550.719
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 242127-03-3.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: t-butyl 3-(2-allyloxycarbonylethyl)-4-methyl-5-({4-methyl-5-oxo-3-[2-(p-tolylthio)ethyl]-1H-pyrrol-2(5H)-ylidene}methyl)-1H-pyrrole-2-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: t-butyl 3-(2-allyloxycarbonylethyl)-4-methyl-5-({4-methyl-5-oxo-3-[2-(p-tolylthio)ethyl]-1H-pyrrol-2(5H)-ylidene}methyl)-1H-pyrrole-2-carboxylate(242127-03-3)
    11. EPA Substance Registry System: t-butyl 3-(2-allyloxycarbonylethyl)-4-methyl-5-({4-methyl-5-oxo-3-[2-(p-tolylthio)ethyl]-1H-pyrrol-2(5H)-ylidene}methyl)-1H-pyrrole-2-carboxylate(242127-03-3)
  • 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: 242127-03-3(Hazardous Substances Data)

242127-03-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 242127-03-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,2,1,2 and 7 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 242127-03:
(8*2)+(7*4)+(6*2)+(5*1)+(4*2)+(3*7)+(2*0)+(1*3)=93
93 % 10 = 3
So 242127-03-3 is a valid CAS Registry Number.

242127-03-3Downstream Products

242127-03-3Relevant articles and documents

Synthesis of doubly locked 5Zs15Za-biliverdin derivatives and their unique spectral behavior

Chen, Liyi,Kinoshita, Hideki,Inomata, Katsuhiko

scheme or table, p. 602 - 603 (2011/04/21)

Doubly locked 5Zs15Zb-biliverdin (BV) derivatives were synthesized toward the investigation of stereochemistry and function of the chromophore in bacteriophytochromes. The unique spectral behavior of the doubly locked 5Zs15Za-BV derivatives was observed b

Syntheses of biliverdin derivatives sterically locked at the CD-ring components

Hammam, Mostafa A. S.,Nakamura, Hiroshi,Hirata, Yukari,Khawn, Htoi,Murata, Yasue,Kinoshita, Hideki,Inomata, Katsuhiko

, p. 1561 - 1572 (2007/10/03)

Total syntheses of biliverdin derivatives with a Z-syn, Z-anti, or E-syn CD-ring components were accomplished via new and efficient methods for the construction of sterically locked CD-ring components towards the elucidation of the stereochemistry of the chromophore in phytochromes.

Total synthesis of (±)-phytochromobilin starting from two pyrrole derivatives

Kakiuchi, Takashi,Kinoshita, Hideki,Inomata, Katsuhiko

, p. 901 - 904 (2007/10/03)

(±)-Phytochromobilin was synthesized as an acid form by developing a convenient method for the preparation of A- and D-rings starting from a 2- tosylpyrrole derivative, followed by efficient construction of A/B- and C/D- ring components via Wittig-type coupling reaction of 5-tosylpyrrolinones with 2-formylpyrrole, and palladium catalyzed deprotection of allyl esters of propanoic acid side chains at C-8 and C-12.

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