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CAS

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153833-01-3

N-acetyl-β-<(1S,4S)-1-hydroxycyclohex-2-en-4-yl>-(S)-alanine 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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  • 153833-01-3 Structure

  • Basic information

    1. Product Name: N-acetyl-β-<(1S,4S)-1-hydroxycyclohex-2-en-4-yl>-(S)-alanine methyl ester
    2. Synonyms: N-acetyl-β-<(1S,4S)-1-hydroxycyclohex-2-en-4-yl>-(S)-alanine methyl ester
    3. CAS NO:153833-01-3
    4. Molecular Formula:
    5. Molecular Weight: 241.287
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 153833-01-3.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: N-acetyl-β-<(1S,4S)-1-hydroxycyclohex-2-en-4-yl>-(S)-alanine methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-acetyl-β-<(1S,4S)-1-hydroxycyclohex-2-en-4-yl>-(S)-alanine methyl ester(153833-01-3)
    11. EPA Substance Registry System: N-acetyl-β-<(1S,4S)-1-hydroxycyclohex-2-en-4-yl>-(S)-alanine methyl ester(153833-01-3)

  • 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: 153833-01-3(Hazardous Substances Data)

153833-01-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 153833-01-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,8,3 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 153833-01:
(8*1)+(7*5)+(6*3)+(5*8)+(4*3)+(3*3)+(2*0)+(1*1)=123
123 % 10 = 3
So 153833-01-3 is a valid CAS Registry Number.

153833-01-3Downstream Products

153833-01-3Relevant articles and documents

Stereocontrolled enantiospecific synthesis of anticapsin

Baldwin, Jack E.,Adlington, Robert M.,Mitchell, Mark B.

, p. 5193 - 5206 (2007/10/02)

A stereocontrolled enantiospecific synthesis of the revised structure of anticapsin (3) is described. The carbonyl group of anticapsin has also been observed to be markedly electrophilic, showing a high propensity for hydration and enolisation. A possible role for the hydrated form of anticapsin during the inhibition of glucosamine synthetase is proposed.

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