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10357-01-4

methyl (methyl α,β-D-galactofuranosid)uronate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 10357-01-4 Structure

  • Basic information

    1. Product Name: methyl (methyl α,β-D-galactofuranosid)uronate
    2. Synonyms:
    3. CAS NO:10357-01-4
    4. Molecular Formula:
    5. Molecular Weight: 222.195
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 10357-01-4.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: methyl (methyl α,β-D-galactofuranosid)uronate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl (methyl α,β-D-galactofuranosid)uronate(10357-01-4)
    11. EPA Substance Registry System: methyl (methyl α,β-D-galactofuranosid)uronate(10357-01-4)

  • 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: 10357-01-4(Hazardous Substances Data)

10357-01-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10357-01-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,5 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 10357-01:
(7*1)+(6*0)+(5*3)+(4*5)+(3*7)+(2*0)+(1*1)=64
64 % 10 = 4
So 10357-01-4 is a valid CAS Registry Number.

10357-01-4Relevant articles and documents

METHANOLYSIS STUDIES OF CARBOHYDRATES, USING H.P.L.C.

Cheetham, Norman W. H.,Sirimanne, Padmini

, p. 1 - 10 (2007/10/02)

An h.p.l.c. system that separates carbohydrates as their methyl glycosides has been used to study the products obtained on treatment of various carbohydrates with methanolic hydrogen chloride.Results are presented for the monosaccharide composition of several polysaccharides, lactone and ester formation during the treatment of D-glucuronic acid, and relative rates of glycosidation vs. esterification during the treatment of D-galacturonic acid.

PROTON AND CARBON-13 NUCLEAR MAGNETIC RESONANCE STUDIES ON METHYL (METHYL D-GALACTOSID)URONATES AND THEIR PER-O-ACETYL DERIVATIVES

Matsuhiro, Bety,Zanlungo, Alberto B.,Dutton, Guy G. S.

, p. 11 - 18 (2007/10/02)

The 1H- and 13C-n.m.r. spectra of the anomeric methyl (methyl D-galactosid)uronates, as well as the 1H-n.m.r. spectra of their acetyl derivatives, were analyzed.The spectra of the unacetylated D-galactopyranosiduronates showed good correlation with those of the corresponding anomeric D-galactopyranuronic acids and their methyl esters, and with those of the anomeric methyl D-galactopyranosides.From the values of the chemical shifts and coupling constants, it was concluded that the anomeric methyl (methyl D-galactopyranosid)uronates and their corrasponding peracetates are in the 4C1(D) conformation.The chemical shifts in the 13C-n.m.r. spectra show good correlation with those of the methyl D-galactosides.The signals of the furanose derivatives appear at fields lower than those of the corresponding pyranose compounds.

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