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CAS

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135908-13-3

2-butylamino-3-tosyl-1-propanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 135908-13-3 Structure

  • Basic information

    1. Product Name: 2-butylamino-3-tosyl-1-propanol
    2. Synonyms:
    3. CAS NO:135908-13-3
    4. Molecular Formula:
    5. Molecular Weight: 285.408
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 135908-13-3.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: 2-butylamino-3-tosyl-1-propanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-butylamino-3-tosyl-1-propanol(135908-13-3)
    11. EPA Substance Registry System: 2-butylamino-3-tosyl-1-propanol(135908-13-3)

  • 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: 135908-13-3(Hazardous Substances Data)

135908-13-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 135908-13-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,9,0 and 8 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 135908-13:
(8*1)+(7*3)+(6*5)+(5*9)+(4*0)+(3*8)+(2*1)+(1*3)=133
133 % 10 = 3
So 135908-13-3 is a valid CAS Registry Number.

135908-13-3Downstream Products

135908-13-3Relevant articles and documents

β,γ-EPOXY SULFONES IN ORGANIC SYNTHESIS. PART 2: PREPARATION OF β,γ-BIFUNCIONALIZED SULFONES

Najera, Carmen,Sansano, Jose M.

, p. 5193 - 5202 (1991)

Heteronucleophiles reagents react with β,γ-epoxy sulfones 1 at the γ position in the presence of Ti(OPri)4 or magnesium halides to afford regioselectively γ-functionalized β-hydroxy sulfones 2.With soft nucleophiles such as sodium azide, triphenylphosphine, or sodium benzethiolate the reaction takes place in the absence of Lewis acids.In the case of basic reagents such as sodium methoxide or diethylamine the corresponding regioisomers, the β-functionalized γ-hydroxy sulfones 3 were exclusively obtained.The preparation of compounds 3 (R2 = H) was also carried out starting from 3-tosyl-2-propen-1-ol (4) by Michael addition of different heteronucleophiles.

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