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8-(Methoxycarbonyl)octyl 2,3,4,6-tetra-O-benzyl-α-D-mannopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 143528-17-0 Structure
  • Basic information

    1. Product Name: 8-(Methoxycarbonyl)octyl 2,3,4,6-tetra-O-benzyl-α-D-mannopyranoside
    2. Synonyms:
    3. CAS NO:143528-17-0
    4. Molecular Formula:
    5. Molecular Weight: 710.908
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 143528-17-0.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: 8-(Methoxycarbonyl)octyl 2,3,4,6-tetra-O-benzyl-α-D-mannopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: 8-(Methoxycarbonyl)octyl 2,3,4,6-tetra-O-benzyl-α-D-mannopyranoside(143528-17-0)
    11. EPA Substance Registry System: 8-(Methoxycarbonyl)octyl 2,3,4,6-tetra-O-benzyl-α-D-mannopyranoside(143528-17-0)
  • 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: 143528-17-0(Hazardous Substances Data)

143528-17-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 143528-17-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,5,2 and 8 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 143528-17:
(8*1)+(7*4)+(6*3)+(5*5)+(4*2)+(3*8)+(2*1)+(1*7)=120
120 % 10 = 0
So 143528-17-0 is a valid CAS Registry Number.

143528-17-0Relevant articles and documents

Glycosidation with 1-hydroxy sugars as glycosyl donors promoted by trimethylsilyl chloride and zinc triflate

Susaki

, p. 1917 - 1918 (1994)

1-Hydroxy sugars (1a-4a) were directly coupled with free alcohols (5b-d) to give the corresponding glycosides by using trimethylsilyl chloride and zinc triflate as promoters.

Novel α-mannoside synthesis promoted by the combination of trimethylsilyl chloride and zinc triflate

Susaki,Higashi

, p. 201 - 204 (2007/10/02)

α-Mannosides were obtained in good yields and with good selectivity directly from benzyl-protected mannopyranosyl p-nitrobenzoate or acetate using a trimethylsilyl chloride-zinc triflate catalyst system.

Synthesis of ω-(methoxycarbonyl)alkyl and 9-(methoxycarbonyl)-3,6-dioxanonyl glycopyranosides for the preparation of carbohydrate-protein conjugates

Sugawara,Irie,Iwasawa,Yoshikawa,Okuno,Watanabe,Kato,Shibukawa,Ito

, p. 117 - 149 (2007/10/02)

ω-(Methoxycarbonyl)alkyl glycopyranosides of D-mannose having C4, C7, C9, C12, and C15 carbon chains, L-fucose and 2-acetamido-2-deoxy-D-mannose having C7 and C9 carbon chains, D

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