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CAS

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873869-10-4

Carbamic acid, [(1R)-2-hydroxy-1-(4-methoxy-7-phenoxy-5-benzofuranyl)ethyl]-, phenylmethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 873869-10-4 Structure

  • Basic information

    1. Product Name: Carbamic acid, [(1R)-2-hydroxy-1-(4-methoxy-7-phenoxy-5-benzofuranyl)ethyl]-, phenylmethyl ester
    2. Synonyms:
    3. CAS NO:873869-10-4
    4. Molecular Formula: C25H23NO6
    5. Molecular Weight: 433.461
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 873869-10-4.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: Carbamic acid, [(1R)-2-hydroxy-1-(4-methoxy-7-phenoxy-5-benzofuranyl)ethyl]-, phenylmethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Carbamic acid, [(1R)-2-hydroxy-1-(4-methoxy-7-phenoxy-5-benzofuranyl)ethyl]-, phenylmethyl ester(873869-10-4)
    11. EPA Substance Registry System: Carbamic acid, [(1R)-2-hydroxy-1-(4-methoxy-7-phenoxy-5-benzofuranyl)ethyl]-, phenylmethyl ester(873869-10-4)

  • 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: 873869-10-4(Hazardous Substances Data)

873869-10-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 873869-10-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,3,8,6 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 873869-10:
(8*8)+(7*7)+(6*3)+(5*8)+(4*6)+(3*9)+(2*1)+(1*0)=224
224 % 10 = 4
So 873869-10-4 is a valid CAS Registry Number.

873869-10-4Relevant articles and documents

Synthesis of arylglycines via the D?tz benzannulation reaction

Pulley, Shon R.,Czakó, Barbara,Brown, Gregory D.

, p. 9039 - 9042 (2007/10/03)

Arylglycines are biologically active α-amino acids. Our approach toward the synthesis of arylglycines features the Do?tz benzannulation reaction between a variety of Fischer chromium carbene complexes 3 and alkyne 4. This leads to the formation of protect

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