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126709-14-6

4-Oxa-1,2-diazaspiro[2.5]oct-1-ene, 6,7,8-tris(phenylmethoxy)-5-[(phenylmethoxy)methyl]-, (5R,6R,7S,8R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • (5R,6R,7S,8R)-6,7,8-Tris(phenylmethoxy)-5-[(phenylmethoxy)methyl]-4-oxa-1,2-diazaspiro[2.5]oct-1-ene

    Cas No: 126709-14-6

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  • 126709-14-6 Structure

  • Basic information

    1. Product Name: 4-Oxa-1,2-diazaspiro[2.5]oct-1-ene, 6,7,8-tris(phenylmethoxy)-5-[(phenylmethoxy)methyl]-, (5R,6R,7S,8R)-
    2. Synonyms:
    3. CAS NO:126709-14-6
    4. Molecular Formula: C34H34N2O5
    5. Molecular Weight: 550.654
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 126709-14-6.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: 4-Oxa-1,2-diazaspiro[2.5]oct-1-ene, 6,7,8-tris(phenylmethoxy)-5-[(phenylmethoxy)methyl]-, (5R,6R,7S,8R)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-Oxa-1,2-diazaspiro[2.5]oct-1-ene, 6,7,8-tris(phenylmethoxy)-5-[(phenylmethoxy)methyl]-, (5R,6R,7S,8R)-(126709-14-6)
    11. EPA Substance Registry System: 4-Oxa-1,2-diazaspiro[2.5]oct-1-ene, 6,7,8-tris(phenylmethoxy)-5-[(phenylmethoxy)methyl]-, (5R,6R,7S,8R)-(126709-14-6)

  • 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: 126709-14-6(Hazardous Substances Data)

126709-14-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126709-14-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,7,0 and 9 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 126709-14:
(8*1)+(7*2)+(6*6)+(5*7)+(4*0)+(3*9)+(2*1)+(1*4)=126
126 % 10 = 6
So 126709-14-6 is a valid CAS Registry Number.

126709-14-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Azi-2,3,4,6-tetra-O-benzyl-1-deoxy-D-glucopyranose

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:126709-14-6 SDS

126709-14-6Relevant articles and documents

Synthesis of endohedral metallofullerene glycoconjugates by carbene addition

Yamada, Michio,Someya, Chika I.,Nakahodo, Tsukasa,Maeda, Yutaka,Tsuchiya, Takahiro,Akasaka, Takeshi

scheme or table, p. 9495 - 9504 (2012/01/05)

Endohedral metallofullerene glycoconjugates were synthesized under mild conditions by carbene addition using appropriate glycosylidene-derived diazirine with La2@Ih-C80. NMR spectroscopic studies revealed that the glycocon

159. Glycosylidene Carbenes - Part 2 - Synthesis of O-Aryl Glycosides

Briner, Karin,Vasella, Andrea

, p. 1764 - 1779 (2007/10/02)

Phenol, 4-methoxyphenol, 4-nitrophenol, methyl orsellinate (1), and 2,6-di(tert-butyl)-4-methylphenol (BHT; 2) have been glycosylated by thermal reaction (20-60 deg C) with various glycosylidene-derived diazirines. 4-Methoxyphenol reacted with the D-gluco

Glycosylidene Carbenes. A New Approach to Glycoside Synthesis. Part 1. Preparation of Glycosylidene-Derived Diaziridines and Diazirines

Briner, Karin,Vasella, Andrea

, p. 1371 - 1382 (2007/10/02)

A new approach towards the synthesis of glycosides based upon a (formal) insertion of glycosylidene carbenes into O-H bonds is presented.The synthesis and characterization of the glycosylidene-derived diazirines 25-28, precursors of glycosylidene carbenes

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