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187732-06-5

allyl 4,6-O-benzylidene-3-O-methyl-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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  • 187732-06-5 Structure

  • Basic information

    1. Product Name: allyl 4,6-O-benzylidene-3-O-methyl-α-D-mannopyranoside
    2. Synonyms: allyl 4,6-O-benzylidene-3-O-methyl-α-D-mannopyranoside
    3. CAS NO:187732-06-5
    4. Molecular Formula:
    5. Molecular Weight: 322.358
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 187732-06-5.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: allyl 4,6-O-benzylidene-3-O-methyl-α-D-mannopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: allyl 4,6-O-benzylidene-3-O-methyl-α-D-mannopyranoside(187732-06-5)
    11. EPA Substance Registry System: allyl 4,6-O-benzylidene-3-O-methyl-α-D-mannopyranoside(187732-06-5)

  • 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: 187732-06-5(Hazardous Substances Data)

187732-06-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 187732-06-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,7,7,3 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 187732-06:
(8*1)+(7*8)+(6*7)+(5*7)+(4*3)+(3*2)+(2*0)+(1*6)=165
165 % 10 = 5
So 187732-06-5 is a valid CAS Registry Number.

187732-06-5Relevant articles and documents

Synthesis of methyl O-α-D-mannosyl-(1→4)-[(3-O-methyl-α-D-mannosyl) -(1→4)-]n3-O-methyl-α-D-mannosides (n = 0, 1, and 2) via dehydrative glycosylation

Hirooka, Motoko,Terayama, Megumi,Mitani, Emi,Koto, Shinkiti,Miura, Asako,Chiba, Kayo,Takabatake, Ayano,Tashiro, Takako

, p. 1301 - 1309 (2002)

Methyl O-α-D-mannopyranosyl-(1→4)-[(3-O-methyl-α-D-mannopyranosyl -(1→4)-]n3-O-methyl-α-D-mannopyra-nosides (n = 0, 1, and 2), the lowest homologs related to the 3-O-methylmannose polysaccharides (MMP) from Mycobacterium smegmatis, were synthesized via dehydrative glycosylation reactions. The reagent systems, composed of p-nitrobenzenesulfonyl chloride, silver trifluoromethanesulfonate, and triethylamine, of p-nitrobenzenesulfonyl chloride, silver trifluoromethanesulfonate, and 1, 8-diazabicyclo[5.4.0]undec-7-ene, and of trimethylsilyl trifuloromethanesulfonate and pyridine were useful.

Synthesis of a hexasaccharide acceptor corresponding to the reducing terminus of mycobacterial 3-O-methylmannose polysaccharide (MMP)

Liao, Wensheng,Lu, Depei

, p. 171 - 182 (2007/10/03)

The title compound methyl O-(2,6-di-O-benzyl-3-O-methyl-α-D-mannopyranosyl)-[( 1 → 4)-O-(2,6-di-O-benzyl-3-O-methyl-α-D-mannopyranosyl)]4-(1 → 4)-2,6-di-O-benzyl-3-O-methyl-α-D mannopyranoside (2) was synthesized in a blockwise manner, employin

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