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2-O-methylrhamnose is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 17212-17-8 Structure
  • Basic information

    1. Product Name: 2-O-methylrhamnose
    2. Synonyms: 2-O-methylrhamnose
    3. CAS NO:17212-17-8
    4. Molecular Formula: C7H14 O5
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 17212-17-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 386.8°Cat760mmHg
    3. Flash Point: 159.7°C
    4. Appearance: /
    5. Density: 1.256g/cm3
    6. Vapor Pressure: 1.4E-07mmHg at 25°C
    7. Refractive Index: 1.487
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-O-methylrhamnose(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-O-methylrhamnose(17212-17-8)
    12. EPA Substance Registry System: 2-O-methylrhamnose(17212-17-8)
  • 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: 17212-17-8(Hazardous Substances Data)

17212-17-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17212-17-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,2,1 and 2 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 17212-17:
(7*1)+(6*7)+(5*2)+(4*1)+(3*2)+(2*1)+(1*7)=78
78 % 10 = 8
So 17212-17-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H14O5/c1-4(9)6(10)7(11)5(3-8)12-2/h3-7,9-11H,1-2H3/t4-,5-,6-,7-/m1/s1

17212-17-8Downstream Products

17212-17-8Relevant articles and documents

O-Alkylated heavy atom carbohydrate probes for protein X-ray crystallography: Studies towards the synthesis of methyl 2-O-methyl-L-selenofucopyranoside

Sommer, Roman,Hauck, Dirk,Varrot, Annabelle,Imberty, Anne,Künzler, Markus,Titz, Alexander

supporting information, p. 2828 - 2833 (2017/01/09)

Selenoglycosides are used as reactive glycosyl donors in the syntheses of oligosaccharides. In addition, such heavy atom analogs of natural glycosides are useful tools for structure determination of their lectin receptors using X-ray crystallography. Some

Structural analysis of the O-polysaccharide of the lipopolysaccharide from Azospirillum brasilense Jm6B2 containing 3-O-methyl-D-rhamnose (D-acofriose)

Boyko, Alevtina S.,Dmitrenok, Andrey S.,Fedonenko, Yuliya P.,Zdorovenko, Evelina L.,Konnova, Svetlana A.,Knirel, Yuriy A.,Ignatov, Vladimir V.

experimental part, p. 92 - 95 (2012/09/07)

Two types of neutral O-polysaccharides were obtained by mild acid degradation of the lipopolysaccharide isolated by phenol-water extraction from the asymbiotic diazotrophic rhizobacterium Azospirillum brasilense Jm6B2. The following structure of the major O-polysaccharide was established by composition and methylation (ethylation) analyses, Smith degradation, and 1D and 2D 1H and 13C NMR spectroscopy: α-D-Rhap3OMe 1↓3→4)-α-L-Fucp-(1→4)-β-D-Xylp-(1→ where a non-stoichiometric (~60%) 3-O-methylation of D-rhamnose is indicated by italics.

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