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637338-96-6

(E)-(S)-5-Benzyloxy-hex-2-enoic acid ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 637338-96-6 Structure

  • Basic information

    1. Product Name: (E)-(S)-5-Benzyloxy-hex-2-enoic acid ethyl ester
    2. Synonyms: (E)-(S)-5-Benzyloxy-hex-2-enoic acid ethyl ester
    3. CAS NO:637338-96-6
    4. Molecular Formula:
    5. Molecular Weight: 248.322
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 637338-96-6.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)-(S)-5-Benzyloxy-hex-2-enoic acid ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-(S)-5-Benzyloxy-hex-2-enoic acid ethyl ester(637338-96-6)
    11. EPA Substance Registry System: (E)-(S)-5-Benzyloxy-hex-2-enoic acid ethyl ester(637338-96-6)

  • 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: 637338-96-6(Hazardous Substances Data)

637338-96-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 637338-96-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,7,3,3 and 8 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 637338-96:
(8*6)+(7*3)+(6*7)+(5*3)+(4*3)+(3*8)+(2*9)+(1*6)=186
186 % 10 = 6
So 637338-96-6 is a valid CAS Registry Number.

637338-96-6Relevant articles and documents

Stereospecific total synthesis of (-)-8-epi-hyperaspine

Ma, Dawei,Zhu, Wei

, p. 8609 - 8612 (2003)

Condensation of protected δ-hydroxy-β-amino ester 7 with a β-keto ester provides vinylogous urethane 8, which is cyclized under the action of t-BuOK followed by decarboxylation to afford enone 12. Hydrogenation of 12 or its N,O-diprotected derivative 13 g

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