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1237517-66-6

4-O-Benzyl Tyrosol α-Acetate 3-Aldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1237517-66-6 Structure

  • Basic information

    1. Product Name: 4-O-Benzyl Tyrosol α-Acetate 3-Aldehyde
    2. Synonyms: 4-O-Benzyl Tyrosol α-Acetate 3-Aldehyde
    3. CAS NO:1237517-66-6
    4. Molecular Formula: C18H18O4
    5. Molecular Weight: 298.33312
    6. EINECS: N/A
    7. Product Categories: Aromatics;Intermediates & Fine Chemicals;Metabolites & Impurities;Pharmaceuticals;Aromatics, Metabolites & Impurities, Pharmaceuticals, Intermediates & Fine Chemicals
    8. Mol File: 1237517-66-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 456.0±40.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.169±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: Dichloromethane, Ethyl Acetate, Methanol, Hexane
    9. CAS DataBase Reference: 4-O-Benzyl Tyrosol α-Acetate 3-Aldehyde(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-O-Benzyl Tyrosol α-Acetate 3-Aldehyde(1237517-66-6)
    11. EPA Substance Registry System: 4-O-Benzyl Tyrosol α-Acetate 3-Aldehyde(1237517-66-6)

  • 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: 1237517-66-6(Hazardous Substances Data)

1237517-66-6 Usage

Chemical Properties

Pale Yellow Oil

Check Digit Verification of cas no

The CAS Registry Mumber 1237517-66-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,7,5,1 and 7 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1237517-66:
(9*1)+(8*2)+(7*3)+(6*7)+(5*5)+(4*1)+(3*7)+(2*6)+(1*6)=156
156 % 10 = 6
So 1237517-66-6 is a valid CAS Registry Number.

1237517-66-6Relevant articles and documents

An efficient, economical synthesis of hydroxytyrosol and its protected forms via Baeyer-Villiger oxidation

Piersanti, Giovanni,Retini, Michele,Espartero, José L.,Madrona, Andres,Zappia, Giovanni

scheme or table, p. 4938 - 4940 (2011/10/07)

An efficient and practical preparation of hydroxytyrosol and its orthogonally-protected forms was developed from inexpensive tyrosol. The utilization of Baeyer-Villiger oxidation enables the chemoselective introduction of a phenolic hydroxyl group in good yield.

N-ACYL ANTHRANILIC ACID DERIVATIVE OR SALT THEREOF

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Page/Page column 26-27, (2011/11/13)

An N-acyl anthranilic acid derivative represented by general formula (1) or a salt thereof is useful for prevention or treatment of diseases associated with excessive production of collagen. (In the formula, R1 represents a carboxyl group or the like; R2 represents a hydrogen atom or the like; R3 represents an optionally substituted aryl group or the like; X1 represents a carbonyl group; X2 represents a bonding hand; X3 represents a bonding hand; X4 represents a bonding hand or the like; and A represents an optionally substituted phenyl group or the like.)

N-ACYL ANTHRANILIC ACID DERIVATIVE OR SALT THEREOF

-

Page/Page column 39-40, (2011/11/13)

An N-acyl anthranilic acid derivative represented by general formula (1) or a salt thereof is useful for prevention or treatment of diseases associated with excessive production of collagen. (In the formula, R1 represents a carboxyl group or th

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