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CAS

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231619-09-3

(2R,3S,4S,5R,6R)-6-azido-2,3-epoxy-4,5,7-tris(benzyloxy)-2(E)-hepten-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 231619-09-3 Structure

  • Basic information

    1. Product Name: (2R,3S,4S,5R,6R)-6-azido-2,3-epoxy-4,5,7-tris(benzyloxy)-2(E)-hepten-1-ol
    2. Synonyms: (2R,3S,4S,5R,6R)-6-azido-2,3-epoxy-4,5,7-tris(benzyloxy)-2(E)-hepten-1-ol
    3. CAS NO:231619-09-3
    4. Molecular Formula:
    5. Molecular Weight: 489.571
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 231619-09-3.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: (2R,3S,4S,5R,6R)-6-azido-2,3-epoxy-4,5,7-tris(benzyloxy)-2(E)-hepten-1-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2R,3S,4S,5R,6R)-6-azido-2,3-epoxy-4,5,7-tris(benzyloxy)-2(E)-hepten-1-ol(231619-09-3)
    11. EPA Substance Registry System: (2R,3S,4S,5R,6R)-6-azido-2,3-epoxy-4,5,7-tris(benzyloxy)-2(E)-hepten-1-ol(231619-09-3)

  • 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: 231619-09-3(Hazardous Substances Data)

231619-09-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 231619-09-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,1,6,1 and 9 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 231619-09:
(8*2)+(7*3)+(6*1)+(5*6)+(4*1)+(3*9)+(2*0)+(1*9)=113
113 % 10 = 3
So 231619-09-3 is a valid CAS Registry Number.

231619-09-3Downstream Products

231619-09-3Relevant articles and documents

Iminocyclitol inhibitors of hexoaminidase and glycosidase

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Page/Page column 13; sheet 5, (2010/02/08)

Designed iminocylitols that have potent inhibition activity with respect to hexominidases and glycosides are disclosed.

A versatile synthetic strategy for the preparation and discovery of new iminocyclitols as inhibitors of glycosidases

Takebayashi, Maki,Hiranuma, Sayoko,Kanie, Yoshimi,Kajimoto, Tetsuya,Kanie, Osamu,Wong, Chi-Huey

, p. 5280 - 5291 (2007/10/03)

A series of iminocyclitols was prepared using a versatile synthetic strategy, and their inhibition of glycosidases was evaluated using capillary electrophoresis. The study has demonstrated that remarkable specificities in enzyme inhibition can be achieved with small modifications on the aglycon side chain and the ring nitrogen. Among the compounds synthesized, (2R,3R,4R,5R)-N-methyl-2(acetamidomethyl)-3,4-dihydroxy-5- (hydroxymethyl)pyrrolidine was found to be very potent against β-N- acetylhexosaminidase P with the K(i) value of 80 nM.

Synthesis and inhibition analysis of five-membered homoazasugars from D-arabinofuranose via an SN2 reaction of the chloromethylsulfonate

Hiranuma,Shimizu,Nakata,Kajimoto,Wong

, p. 8247 - 8250 (2007/10/02)

Five-membered homoazasugars having a side-chain which can be modified to other functional groups or linked to other aglycon moieties were prepared from 2,3,5-tri-O-benzyl-D-arabinofuranose via a favorable SN2 reaction of the chloromethylsulfonate with azi

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