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CAS

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877670-98-9

(E)-(2S,3S)-2-Benzyloxy-3-phenyl-hept-4-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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  • 877670-98-9 Structure

  • Basic information

    1. Product Name: (E)-(2S,3S)-2-Benzyloxy-3-phenyl-hept-4-enoic acid methyl ester
    2. Synonyms:
    3. CAS NO:877670-98-9
    4. Molecular Formula:
    5. Molecular Weight: 324.42
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 877670-98-9.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)-(2S,3S)-2-Benzyloxy-3-phenyl-hept-4-enoic acid methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-(2S,3S)-2-Benzyloxy-3-phenyl-hept-4-enoic acid methyl ester(877670-98-9)
    11. EPA Substance Registry System: (E)-(2S,3S)-2-Benzyloxy-3-phenyl-hept-4-enoic acid methyl ester(877670-98-9)

  • 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: 877670-98-9(Hazardous Substances Data)

877670-98-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 877670-98-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,7,6,7 and 0 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 877670-98:
(8*8)+(7*7)+(6*7)+(5*6)+(4*7)+(3*0)+(2*9)+(1*8)=239
239 % 10 = 9
So 877670-98-9 is a valid CAS Registry Number.

877670-98-9Relevant articles and documents

Efficient enantioselective synthesis of α-hydroxy-β-amino acids using the Claisen and Curtius rearrangements

Jung, Doo Young,Kang, Sol,Chang, Sukbok,Kim, Yong Hae

, p. 86 - 90 (2006)

Highly enantioselective and facile synthesis of α-hydroxy-β- amino acids has been achieved using the Claisen and Curtius rearrangements as key reactions. Chiral allylic alcohols were employed, which can be prepared by asymmetric catalysis in both E- and Z

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