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4-Benzyl 1-t-Butyl N-t-Butyloxycarbonyl-N-ethoxycarbonylmethyl-L-aspartate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 125989-84-6 Structure
  • Basic information

    1. Product Name: 4-Benzyl 1-t-Butyl N-t-Butyloxycarbonyl-N-ethoxycarbonylmethyl-L-aspartate
    2. Synonyms: 4-Benzyl 1-t-Butyl N-t-Butyloxycarbonyl-N-ethoxycarbonylmethyl-L-aspartate
    3. CAS NO:125989-84-6
    4. Molecular Formula:
    5. Molecular Weight: 465.544
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 125989-84-6.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: 4-Benzyl 1-t-Butyl N-t-Butyloxycarbonyl-N-ethoxycarbonylmethyl-L-aspartate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-Benzyl 1-t-Butyl N-t-Butyloxycarbonyl-N-ethoxycarbonylmethyl-L-aspartate(125989-84-6)
    11. EPA Substance Registry System: 4-Benzyl 1-t-Butyl N-t-Butyloxycarbonyl-N-ethoxycarbonylmethyl-L-aspartate(125989-84-6)
  • 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: 125989-84-6(Hazardous Substances Data)

125989-84-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 125989-84-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,9,8 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 125989-84:
(8*1)+(7*2)+(6*5)+(5*9)+(4*8)+(3*9)+(2*8)+(1*4)=176
176 % 10 = 6
So 125989-84-6 is a valid CAS Registry Number.

125989-84-6Downstream Products

125989-84-6Relevant articles and documents

On pyrrolidine derivatives I. An efficient synthesis of 3-substituted (2S,5S)-pyrrolidine-2,5-dicarboxylic acids

Honma,Tada,Adachi,Igarashi

, p. 629 - 634 (2007/10/02)

(2S,5S)-3-Alkylpyrrolidine-2,5-dicarboxylic acid derivatives I were stereoselectively synthesized by means of an efficient method starting from L-aspartic acid. (1) Dieckmann reaction of 4-benzyl l-t-butyl N-t-butyl-oxycarbonyl-N-ethoxycarbonylmethyl-L-as

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