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(S)-3-azido-1-phenyl-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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  • 357434-40-3 Structure
  • Basic information

    1. Product Name: (S)-3-azido-1-phenyl-1-propanol
    2. Synonyms: (S)-3-azido-1-phenyl-1-propanol
    3. CAS NO:357434-40-3
    4. Molecular Formula:
    5. Molecular Weight: 177.206
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 357434-40-3.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: (S)-3-azido-1-phenyl-1-propanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-3-azido-1-phenyl-1-propanol(357434-40-3)
    11. EPA Substance Registry System: (S)-3-azido-1-phenyl-1-propanol(357434-40-3)
  • 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: 357434-40-3(Hazardous Substances Data)

357434-40-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 357434-40-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,7,4,3 and 4 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 357434-40:
(8*3)+(7*5)+(6*7)+(5*4)+(4*3)+(3*4)+(2*4)+(1*0)=153
153 % 10 = 3
So 357434-40-3 is a valid CAS Registry Number.

357434-40-3Relevant articles and documents

A Green approach towards the synthesis of chiral alcohols using functionalized alginate immobilized Saccharomyces cerevisiae cells

Muthineni, Narmada,Arnipally, Manikanta Swamy,Bojja, Sridhar,Meshram, Harshadas Mitaram,Srivastava, Ajay Kumar,Adari, Bhaskar Rao

, p. 233 - 237 (2016)

The stereochemistry of the drug molecule is gaining greater therapeutic importance and thus much attention was drawn in synthesis of chiral compounds by the pharmaceutical industry. In this study Saccharomyces cerevisiae cells immobilized on functionalize

Chemoenzymatic synthesis of fluoxetine precursors. Reduction of β-substituted propiophenones

Coronel, Camila,Arce, Gabriel,Iglesias, Cesar,Noguera, Cynthia Magallanes,Bonnecarrere, Paula Rodriguez,Giordano, Sonia Rodriguez,Gonzalez, David

, p. 94 - 98 (2014/03/21)

Five endophytic yeast strains isolated from edible plants were tested in the reduction β-chloro- and β-azidopropiophenone for the preparation of optically active fluoxetine precursors. The biotransformation rendered not only the corresponding chiral γ-substituted alcohols, but also unsubstituted alcohols and ketones. The product profile was studied and a plausible mechanism for the reductive elimination of the β-functional group is proposed.

Synthesis of enantiomerically pure γ-azidoalcohols by lipase-catalyzed transesterification

Kamal, Ahmed,Malik, M. Shaheer,Shaik, Ahmad Ali,Azeeza, Shaik

, p. 1078 - 1083 (2008/09/19)

An enantioselective synthesis of chiral γ-azidoalcohols via lipase-catalyzed resolution is described. The efficiency of various lipases and the effect of different solvents have been studied. Pseudomonas cepacia immobilized on diatomaceous earth (PS-D) in n-hexane catalyzed the transesterification process in an efficient manner providing γ-azidoalcohols in high enantiomeric excess.

[3H]-(R)-NPTS, a radioligand for the type 1 glycine transporter.

Lowe 3rd., John A,Drozda, Susan E,Fisher, Katherine,Strick, Christine,Lebel, Lorraine,Schmidt, Christopher,Hiller, Donna,Zandi, Kathleen S

, p. 1291 - 1292 (2007/10/03)

The synthesis of NPTS, 6, a potent inhibitor of the type 1 glycine transporter (GlyT1) is described, as well as preparation of 6 in optically active and tritiated form for use as a radioligand for affinity displacement assay of GlyT1.

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