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CAS

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228867-83-2

(S)-1-(benzyloxycarbonyl)-2-azetidinemethanol-p-tosylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 228867-83-2 Structure

  • Basic information

    1. Product Name: (S)-1-(benzyloxycarbonyl)-2-azetidinemethanol-p-tosylate
    2. Synonyms: (S)-1-(benzyloxycarbonyl)-2-azetidinemethanol-p-tosylate
    3. CAS NO:228867-83-2
    4. Molecular Formula:
    5. Molecular Weight: 375.445
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 228867-83-2.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: (S)-1-(benzyloxycarbonyl)-2-azetidinemethanol-p-tosylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-1-(benzyloxycarbonyl)-2-azetidinemethanol-p-tosylate(228867-83-2)
    11. EPA Substance Registry System: (S)-1-(benzyloxycarbonyl)-2-azetidinemethanol-p-tosylate(228867-83-2)

  • 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: 228867-83-2(Hazardous Substances Data)

228867-83-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 228867-83-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,8,8,6 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 228867-83:
(8*2)+(7*2)+(6*8)+(5*8)+(4*6)+(3*7)+(2*8)+(1*3)=182
182 % 10 = 2
So 228867-83-2 is a valid CAS Registry Number.

228867-83-2Downstream Products

228867-83-2Relevant articles and documents

Synthesis of a new precursor to the nicotinic receptor tracer 5-IA-85380 precursor using trimethylsilyl iodide as deblocking agent

Brenner, Eric,Baldwin, Ronald M.,Tamagnan, Gilles

, p. 3607 - 3610 (2004)

We describe the synthesis of a new precursor of 5-IA-85380, specific radiotracer for α4β2 nicotinic acetylcholine receptors. (S)-5-Trimethylstannyl-3-(2-azetidinylmethoxy)pyridine (4) was prepared in six steps and 62% overall yield starting from (S)-2- azetidinecarboxylic acid. The key step of this synthesis is selective release of the amine function without removing the stannyl moiety using trimethylsilyl iodine.

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