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3,4,5-trimethoxyphenyl 6-O-(5-O-benzyl-β-D-erythro-apiofuranosyl)-β-D-glucopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 3,4,5-trimethoxyphenyl 6-O-(5-O-benzyl-β-D-erythro-apiofuranosyl)-β-D-glucopyranoside

    Cas No: 209113-72-4

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  • 209113-72-4 Structure
  • Basic information

    1. Product Name: 3,4,5-trimethoxyphenyl 6-O-(5-O-benzyl-β-D-erythro-apiofuranosyl)-β-D-glucopyranoside
    2. Synonyms: 3,4,5-trimethoxyphenyl 6-O-(5-O-benzyl-β-D-erythro-apiofuranosyl)-β-D-glucopyranoside
    3. CAS NO:209113-72-4
    4. Molecular Formula:
    5. Molecular Weight: 568.575
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 209113-72-4.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: 3,4,5-trimethoxyphenyl 6-O-(5-O-benzyl-β-D-erythro-apiofuranosyl)-β-D-glucopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,4,5-trimethoxyphenyl 6-O-(5-O-benzyl-β-D-erythro-apiofuranosyl)-β-D-glucopyranoside(209113-72-4)
    11. EPA Substance Registry System: 3,4,5-trimethoxyphenyl 6-O-(5-O-benzyl-β-D-erythro-apiofuranosyl)-β-D-glucopyranoside(209113-72-4)
  • 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: 209113-72-4(Hazardous Substances Data)

209113-72-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 209113-72-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,9,1,1 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 209113-72:
(8*2)+(7*0)+(6*9)+(5*1)+(4*1)+(3*3)+(2*7)+(1*2)=104
104 % 10 = 4
So 209113-72-4 is a valid CAS Registry Number.

209113-72-4Relevant articles and documents

An expeditious route to the synthesis of kelampayosides A and B

Duynstee, Howard I.,De Koning, Martijn C.,Van der Marel, Gijs A.,Van Boom, Jacques H.

, p. 9881 - 9898 (2007/10/03)

Chemoselective NIS/cat. TfOH-mediated glycosylation of ethyl 2,3,4-tri- O-benzoyl-1-thio-β-D-glucopyranoside (13) with ethyl 2,3-di-O-acetyl-5-O- benzyl-1-thio-α/β-erythro-apiofuranoside (4a) gave direct 14 in an excellent yield. BF3·Et2O-catalysed condensation of the α- trichloroacetimidate 31, accessible in two steps from 14, with 3,4,5- trimethoxyphenol gave β-linked derivative 32 followed by deprotection gave Kelampayoside A. Protecting group manipulations of 32 and subsequent caffeoylation of resulting 36 followed by deprotection gave Kelampayoside B.

Synthesis of 3,4,5-trimethoxyphenyl 5-O-caffeoyl-β-D-erythro- apiofuranosyl-(1→6)-β D-glucopyranoside: Kelampayoside B

Duynstee, Howard I.,De Koning, Martijn C.,Van Der Marel, Gijs A.,Van Boom, Jacques H.

, p. 4129 - 4132 (2007/10/03)

Chemoselective NIS/cat. TfOH-mediated glycosylation of ethyl 2,3,4-tri- O-benzoyl-1-thio-β-D-glucopyranoside (4) with ethyl 2,3-di-O-acetyl-5-O- benzyl-1-thio-β-D-erythro-apiofuranoside (3) gave dimer 5 in an excellent yield. BF3Et2O-catalysed condensation of the α-trichloroacetimidate 18, accessible in two steps from 5, with 3,4,5-trimethoxyphenol gave β-linked derivative 19 which could be transformed in five steps into the title compound.

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