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2,6-Heptadienoic acid, 3,5-dimethoxy-4-methyl-7-phenyl-, methyl ester, (2E,4R,5S,6E)is a methyl ester derivative of 2,6-heptadienoic acid with a complex chemical structure featuring a carboxylic acid, a double bond, and a phenyl group. The presence of two methoxy groups and a methyl group in the molecule suggests potential applications in various fields, such as organic synthesis, pharmaceuticals, or as a precursor for the synthesis of other compounds. The specific configuration of the double bonds (2E,6E) and the stereochemistry (4R,5S) are crucial for its chemical reactivity and potential biological activity. Further research and analysis are needed to fully understand the properties and potential uses of this compound.

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  • 478011-19-7 Structure
  • Basic information

    1. Product Name: 2,6-Heptadienoic acid, 3,5-dimethoxy-4-methyl-7-phenyl-, methyl ester, (2E,4R,5S,6E)-
    2. Synonyms:
    3. CAS NO:478011-19-7
    4. Molecular Formula: C17H22O4
    5. Molecular Weight: 290.359
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 478011-19-7.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: 2,6-Heptadienoic acid, 3,5-dimethoxy-4-methyl-7-phenyl-, methyl ester, (2E,4R,5S,6E)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,6-Heptadienoic acid, 3,5-dimethoxy-4-methyl-7-phenyl-, methyl ester, (2E,4R,5S,6E)-(478011-19-7)
    11. EPA Substance Registry System: 2,6-Heptadienoic acid, 3,5-dimethoxy-4-methyl-7-phenyl-, methyl ester, (2E,4R,5S,6E)-(478011-19-7)
  • 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: 478011-19-7(Hazardous Substances Data)

478011-19-7 Usage

Uses

Used in Organic Synthesis:
2,6-Heptadienoic acid, 3,5-dimethoxy-4-methyl-7-phenyl-, methyl ester, (2E,4R,5S,6E)is used as a building block in organic synthesis for the creation of various complex organic compounds. Its unique structure, including the carboxylic acid, double bond, and phenyl group, allows for versatile chemical reactions and the formation of a wide range of products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,6-Heptadienoic acid, 3,5-dimethoxy-4-methyl-7-phenyl-, methyl ester, (2E,4R,5S,6E)is used as a precursor for the synthesis of pharmaceutical compounds. Its specific configuration and functional groups may contribute to the development of new drugs with unique properties and therapeutic effects.
Used in Chemical Research:
2,6-Heptadienoic acid, 3,5-dimethoxy-4-methyl-7-phenyl-, methyl ester, (2E,4R,5S,6E)is utilized in chemical research to study its chemical reactivity, stereochemistry, and potential biological activity. Understanding the properties and behavior of this compound can provide valuable insights into the development of new synthetic methods, pharmaceuticals, and other applications.
Used in Material Science:
In the field of material science, 2,6-Heptadienoic acid, 3,5-dimethoxy-4-methyl-7-phenyl-, methyl ester, (2E,4R,5S,6E)may be used as a component in the development of new materials with specific properties. Its unique structure and functional groups can contribute to the creation of materials with tailored characteristics for various applications, such as sensors, catalysts, or advanced materials for specific industries.

Check Digit Verification of cas no

The CAS Registry Mumber 478011-19-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,8,0,1 and 1 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 478011-19:
(8*4)+(7*7)+(6*8)+(5*0)+(4*1)+(3*1)+(2*1)+(1*9)=147
147 % 10 = 7
So 478011-19-7 is a valid CAS Registry Number.

478011-19-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (+)-E-2,E-6-(4R,5S)-3,5-dimethoxy-4-methyl-7-phenyl-hepta-2,6-dienoic acid methyl ester

1.2 Other means of identification

Product number -
Other names (2E,6E)-(4R,5S)-3,5-Dimethoxy-4-methyl-7-phenyl-hepta-2,6-dienoic acid methyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:478011-19-7 SDS

478011-19-7Downstream Products

478011-19-7Relevant articles and documents

Total synthesis of myxothiazols, novel bis-thiazole β-methoxyacrylate- based anti-fungal compounds from myxobacteria

Clough, John M.,Dube, Henry,Martin, Bruce J.,Pattenden, Gerald,Reddy, K. Srinivasa,Waldron, Ian R.

, p. 2906 - 2911 (2008/02/09)

Convergent total syntheses of myxothiazols A and Z are described. The syntheses are based on elaboration of the (S)-E,E-diene thioamide 22, conversion of 22 into the bis-thiazole 27 and Wittig reactions between 27c and the aldehyde 30. The substituted β-m

The first synthesis and antifungal activities of 9-methoxystrobilurin-type β-substituted β-Methoxyacrylate

Uchiro, Hiromi,Nagasawa, Koh,Kotake, Tomoya,Hasegawa, Daiju,Tomita, Aya,Kobayashi, Susumu

, p. 2821 - 2824 (2007/10/03)

The first synthesis of 9-methoxystrobilurin-type β-substituted MOAs was successfully achieved. A chiral oudemansin-type β-substituted MOA was also synthesized utilizing Mukaiyama's asymmetric aldol reaction. Antifungal activities of the synthesized compounds against several representative fungi were examined by disk-diffusion assay. As a result, unique and superior antifungal properties of 9-methoxystrobilurin-type β-substituted MOAs compared with those of oudemansin-type analogue were clearly revealed.

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