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CAS

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78464-49-0

(Z)-2-[(Z)-2-(Benzyloxycarbonylamino)-2-butenoylamino]-2-butenoic 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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  • 78464-49-0 Structure

  • Basic information

    1. Product Name: (Z)-2-[(Z)-2-(Benzyloxycarbonylamino)-2-butenoylamino]-2-butenoic acid methyl ester
    2. Synonyms: (Z)-2-[(Z)-2-(Benzyloxycarbonylamino)-2-butenoylamino]-2-butenoic acid methyl ester
    3. CAS NO:78464-49-0
    4. Molecular Formula:
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 78464-49-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (Z)-2-[(Z)-2-(Benzyloxycarbonylamino)-2-butenoylamino]-2-butenoic acid methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: (Z)-2-[(Z)-2-(Benzyloxycarbonylamino)-2-butenoylamino]-2-butenoic acid methyl ester(78464-49-0)
    11. EPA Substance Registry System: (Z)-2-[(Z)-2-(Benzyloxycarbonylamino)-2-butenoylamino]-2-butenoic acid methyl ester(78464-49-0)

  • 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: 78464-49-0(Hazardous Substances Data)

78464-49-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78464-49-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,4,6 and 4 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 78464-49:
(7*7)+(6*8)+(5*4)+(4*6)+(3*4)+(2*4)+(1*9)=170
170 % 10 = 0
So 78464-49-0 is a valid CAS Registry Number.

78464-49-0Downstream Products

78464-49-0Relevant articles and documents

Dehydrooligopeptides. III. Synthesis of (Z,Z)- and (Z,E)-Geometric Isomers of Dehydrodipeptides and Their Base-catalyzed Transformation to the Hydantoin Derivatives

Shin, Chung-gi,Yonezawa, Yasuhika,Yamada, Toyofumi,Yoshimura, Juji

, p. 2147 - 2152 (1982)

N-Benzyloxycarbonyl (Cbz)-(Z,E)-dehydrodipeptides, comprised of both (Z)- and (E)-α-dehydroamino acid residues, were first synthesized by dehydrochlorination of Cbz-(Z)-dehydrodipeptides containing an erythro-3-chloro-2-aminobutanoate moiety.Base-catalyzed transformation of the individual Cbz-(Z, Z)- and (Z, E)-dehydrodipeptides was carried out to give the corresponding new hydantoin derivatives.The NMR spectroscopic differences between the geometric isomers of both dehydrodipeptides and their hydantoin derivatives were elucidated.

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