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121925-61-9

2-Benzyloxy-succinic acid 1-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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  • 121925-61-9 Structure

  • Basic information

    1. Product Name: 2-Benzyloxy-succinic acid 1-ethyl ester
    2. Synonyms:
    3. CAS NO:121925-61-9
    4. Molecular Formula:
    5. Molecular Weight: 252.267
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 121925-61-9.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: 2-Benzyloxy-succinic acid 1-ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Benzyloxy-succinic acid 1-ethyl ester(121925-61-9)
    11. EPA Substance Registry System: 2-Benzyloxy-succinic acid 1-ethyl ester(121925-61-9)

  • 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: 121925-61-9(Hazardous Substances Data)

121925-61-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 121925-61-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,9,2 and 5 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 121925-61:
(8*1)+(7*2)+(6*1)+(5*9)+(4*2)+(3*5)+(2*6)+(1*1)=109
109 % 10 = 9
So 121925-61-9 is a valid CAS Registry Number.

121925-61-9Downstream Products

121925-61-9Relevant articles and documents

HIGHLY REGIOSELECTIVE RING-OPENING OF α-SUBSTITUTED CYCLIC ACID ANHYDRIDES CATALYZED BY LIPASE

Hiratake, Jun,Yamamoto, Kazuyoshi,Yamamoto, Yukio,Oda, Jun'ichi

, p. 1555 - 1556 (2007/10/02)

Lipase Amano P irreversibly catalyzed a ring-opening of α-substituted cyclic acid anhydrides 1 preferentially at the less hindered carbonyl group to give monoesters with high regioselectivity.

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