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CAS

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315203-56-6

N-(1-deoxo-2,3:4,6-di-O-isoprpylidene-α-L-xylo-hex-2-ul-1-ylidene)benzylamine N-oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 315203-56-6 Structure

  • Basic information

    1. Product Name: N-(1-deoxo-2,3:4,6-di-O-isoprpylidene-α-L-xylo-hex-2-ul-1-ylidene)benzylamine N-oxide
    2. Synonyms: N-(1-deoxo-2,3:4,6-di-O-isoprpylidene-α-L-xylo-hex-2-ul-1-ylidene)benzylamine N-oxide
    3. CAS NO:315203-56-6
    4. Molecular Formula:
    5. Molecular Weight: 363.411
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 315203-56-6.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: N-(1-deoxo-2,3:4,6-di-O-isoprpylidene-α-L-xylo-hex-2-ul-1-ylidene)benzylamine N-oxide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(1-deoxo-2,3:4,6-di-O-isoprpylidene-α-L-xylo-hex-2-ul-1-ylidene)benzylamine N-oxide(315203-56-6)
    11. EPA Substance Registry System: N-(1-deoxo-2,3:4,6-di-O-isoprpylidene-α-L-xylo-hex-2-ul-1-ylidene)benzylamine N-oxide(315203-56-6)

  • 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: 315203-56-6(Hazardous Substances Data)

315203-56-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 315203-56-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,5,2,0 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 315203-56:
(8*3)+(7*1)+(6*5)+(5*2)+(4*0)+(3*3)+(2*5)+(1*6)=96
96 % 10 = 6
So 315203-56-6 is a valid CAS Registry Number.

315203-56-6Downstream Products

315203-56-6Relevant articles and documents

A new version of the reverse-Cope elimination initiated by the nucleophilic addition of allylamines to nitrones: A synthesis of vicinal diamines

Gravestock, Michael B.,Knight, David W.,Abdul Malik,Thornton, Steven R.

, p. 3292 - 3305 (2000)

Attempts to utilize the sugar-derived nitrones 1 in enantioselective [1,3]dipolar cycloadditions with protected aliylamines 6 are only partly successful, giving mixtures of the expected adducts 7. However, reactions between nitrones 1 and unprotected ally

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