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1094172-73-2

C43H46N4O9S3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1094172-73-2 Structure

  • Basic information

    1. Product Name: C43H46N4O9S3
    2. Synonyms: C43H46N4O9S3
    3. CAS NO:1094172-73-2
    4. Molecular Formula:
    5. Molecular Weight: 859.058
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1094172-73-2.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: C43H46N4O9S3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C43H46N4O9S3(1094172-73-2)
    11. EPA Substance Registry System: C43H46N4O9S3(1094172-73-2)

  • 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: 1094172-73-2(Hazardous Substances Data)

1094172-73-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1094172-73-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,4,1,7 and 2 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1094172-73:
(9*1)+(8*0)+(7*9)+(6*4)+(5*1)+(4*7)+(3*2)+(2*7)+(1*3)=152
152 % 10 = 2
So 1094172-73-2 is a valid CAS Registry Number.

1094172-73-2Relevant articles and documents

Synthetic studies on dragmacidin D: Synthesis and assembly of three fragments towards an advanced intermediate

Oikawa, Masato,Ikoma, Minoru,Sasaki, Makoto

, p. 4654 - 4666 (2011/10/03)

We report herein the approach to the key advanced intermediate in the synthesis of the bioactive marine natural product dragmacidin D. By employing a modular synthesis strategy of three fragments (5, 7, and 8), the advanced intermediate 3 has been successfully synthesized in 2.5% yield over 15 steps by starting from nitrotoluene 20. The synthesis also involves sequential cross-coupling reactions, namely Sonogashira and Suzuki-Miyaura reactions, so that various analogues can be efficiently synthesized, which will allow the study of structure-activity relationships of dragmacidin D.

Synthetic studies on dragmacidin D: synthesis of the left-hand fragment

Ikoma, Minoru,Oikawa, Masato,Sasaki, Makoto

scheme or table, p. 7197 - 7199 (2009/04/11)

We report a synthesis of a left-hand fragment of bis(indole)-class marine alkaloid, dragmacidin D. The synthesis features Suzuki-Miyaura reaction for the coupling of imidazolyl boronic acid and (4-indolyl)vinyl bromide.

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