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ethyl p-<4-azido-2-(tert-butoxycarbonyl)amino-2,4,6-trideoxy-α-D-glucopyranosyloxy>cinnamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 83022-03-1 Structure
  • Basic information

    1. Product Name: ethyl p-<4-azido-2-(tert-butoxycarbonyl)amino-2,4,6-trideoxy-α-D-glucopyranosyloxy>cinnamate
    2. Synonyms: ethyl p-<4-azido-2-(tert-butoxycarbonyl)amino-2,4,6-trideoxy-α-D-glucopyranosyloxy>cinnamate
    3. CAS NO:83022-03-1
    4. Molecular Formula:
    5. Molecular Weight: 462.503
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 83022-03-1.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: ethyl p-<4-azido-2-(tert-butoxycarbonyl)amino-2,4,6-trideoxy-α-D-glucopyranosyloxy>cinnamate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl p-<4-azido-2-(tert-butoxycarbonyl)amino-2,4,6-trideoxy-α-D-glucopyranosyloxy>cinnamate(83022-03-1)
    11. EPA Substance Registry System: ethyl p-<4-azido-2-(tert-butoxycarbonyl)amino-2,4,6-trideoxy-α-D-glucopyranosyloxy>cinnamate(83022-03-1)
  • 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: 83022-03-1(Hazardous Substances Data)

83022-03-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83022-03-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,0,2 and 2 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 83022-03:
(7*8)+(6*3)+(5*0)+(4*2)+(3*2)+(2*0)+(1*3)=91
91 % 10 = 1
So 83022-03-1 is a valid CAS Registry Number.

83022-03-1Relevant articles and documents

SYNTHETIC STUDIES ON GLYCOCINNAMOYLSPERMIDINES. SYNTHESIS OF A KEY INTERMEDIATE OF THE DIAMINOHEXOSE MOIETY: ETHYL p-CINNAMATE

Araki, Koichi,Hashimoto, Hironobu,Yoshimura, Juji

, p. 143 - 160 (2007/10/02)

A key synthetic intermediate for the diaminohexosyloxycinnamate moiety of glycocinnamoylspermidines was synthesized from D-galactose by two routes, via 3,4,6-tri-O-acetyl-2-azido-2-deoxy-D-galactopyranosyl nitrate (20) and via 1,6-anhydro-2-azido-2-deoxy-

SYNTHETIC KEY INTERMEDIATES OF GLYCOCINNAMOYLSPERMIDINES ; DIAMINOHEXOSYLOXYCINNAMATE AND AMINOPENTOSE DISACCHARIDE MOIETIES

Araki, Koichi,Miyazawa, Ken-ichi,Hashimoto, Hironobu,Yoshimura, Juji

, p. 1705 - 1708 (2007/10/02)

Two key intermediates for the total synthesis of glycocinnamoylspermidines were derived from the corresponding 2-azido sugars.

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