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Heptanamide, N-methoxy-5-[(4-methoxyphenyl)methoxy]-N,3,6,6-tetramethyl-, (3R,5S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 676324-78-0 Structure
  • Basic information

    1. Product Name: Heptanamide, N-methoxy-5-[(4-methoxyphenyl)methoxy]-N,3,6,6-tetramethyl-, (3R,5S)-
    2. Synonyms:
    3. CAS NO:676324-78-0
    4. Molecular Formula: C20H33NO4
    5. Molecular Weight: 351.486
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 676324-78-0.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: Heptanamide, N-methoxy-5-[(4-methoxyphenyl)methoxy]-N,3,6,6-tetramethyl-, (3R,5S)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Heptanamide, N-methoxy-5-[(4-methoxyphenyl)methoxy]-N,3,6,6-tetramethyl-, (3R,5S)-(676324-78-0)
    11. EPA Substance Registry System: Heptanamide, N-methoxy-5-[(4-methoxyphenyl)methoxy]-N,3,6,6-tetramethyl-, (3R,5S)-(676324-78-0)
  • 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: 676324-78-0(Hazardous Substances Data)

676324-78-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 676324-78-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,6,3,2 and 4 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 676324-78:
(8*6)+(7*7)+(6*6)+(5*3)+(4*2)+(3*4)+(2*7)+(1*8)=190
190 % 10 = 0
So 676324-78-0 is a valid CAS Registry Number.

676324-78-0Downstream Products

676324-78-0Relevant articles and documents

MACROCYCLIC THERAPEUTIC AGENTS, METHODS OF MANUFACTURE, AND METHODS OF TREATMENT

-

, (2015/09/28)

The instant invention describes macrocyclic compounds having therapeutic activity, and the mechanism and methods of treating disorders such as autoimmune diseases, inflammation, and cancer, tumors and cell proliferation related disorders.

Improved total synthesis and biological evaluation of potent apratoxin S4 based anticancer agents with differential stability and further enhanced activity

Chen, Qi-Yin,Liu, Yanxia,Cai, Weijing,Luesch, Hendrik

, p. 3011 - 3029 (2014/05/06)

Apratoxins are cytotoxic natural products originally isolated from marine cyanobacteria that act by preventing cotranslational translocation early in the secretory pathway to downregulate receptor levels and inhibit growth factor secretion, leading to pot

Synthesis of the polyketide segment of apratoxin A

Xu, Zhengshuang,Chen, Zhiyong,Ye, Tao

, p. 355 - 363 (2007/10/03)

Apratoxin A 1 is a potent cytotoxic agent extracted from a marine cyanobacterium. We report the results of our synthetic approaches to the polyketide segment 3-OTBS-7-OPMB-2,5,8,8-tetramethylnonanoic acid 4, and the scope and limitations of these approach

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