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CAS

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161726-04-1

(E)-6-Benzyloxy-4-hydroxy-hex-2-enoic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 161726-04-1 Structure

  • Basic information

    1. Product Name: (E)-6-Benzyloxy-4-hydroxy-hex-2-enoic acid methyl ester
    2. Synonyms: (E)-6-Benzyloxy-4-hydroxy-hex-2-enoic acid methyl ester
    3. CAS NO:161726-04-1
    4. Molecular Formula:
    5. Molecular Weight: 250.295
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 161726-04-1.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: (E)-6-Benzyloxy-4-hydroxy-hex-2-enoic acid methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-6-Benzyloxy-4-hydroxy-hex-2-enoic acid methyl ester(161726-04-1)
    11. EPA Substance Registry System: (E)-6-Benzyloxy-4-hydroxy-hex-2-enoic acid methyl ester(161726-04-1)

  • 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: 161726-04-1(Hazardous Substances Data)

161726-04-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 161726-04-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,7,2 and 6 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 161726-04:
(8*1)+(7*6)+(6*1)+(5*7)+(4*2)+(3*6)+(2*0)+(1*4)=121
121 % 10 = 1
So 161726-04-1 is a valid CAS Registry Number.

161726-04-1Upstream product

161726-04-1Relevant articles and documents

Synthesis of (+)-methyl (R,E)-6-benzyloxy-4-hydroxy-2-hexenoate and its mesylate derivative

De March,Figueredo,Font,Monsalvatje

, p. 331 - 342 (1995)

Methyl (E)-6-benzyloxy-4-hydroxy-2-hexenoate is prepared in both racemic and enantiopure form through reaction between (2-benzyloxy)ethyloxirane and the dianion of phenylselenoacetic acid followed by esterification with diazomethane, oxidation to the selenoxide and subsequent pyrolysis in 72% overall yield.

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