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79083-36-6

methyl 5-O-benzyl-β-D-xylofuranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 79083-36-6 Structure

  • Basic information

    1. Product Name: methyl 5-O-benzyl-β-D-xylofuranoside
    2. Synonyms: methyl 5-O-benzyl-β-D-xylofuranoside
    3. CAS NO:79083-36-6
    4. Molecular Formula:
    5. Molecular Weight: 254.283
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 79083-36-6.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 5-O-benzyl-β-D-xylofuranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 5-O-benzyl-β-D-xylofuranoside(79083-36-6)
    11. EPA Substance Registry System: methyl 5-O-benzyl-β-D-xylofuranoside(79083-36-6)

  • 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: 79083-36-6(Hazardous Substances Data)

79083-36-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79083-36-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,0,8 and 3 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 79083-36:
(7*7)+(6*9)+(5*0)+(4*8)+(3*3)+(2*3)+(1*6)=156
156 % 10 = 6
So 79083-36-6 is a valid CAS Registry Number.

79083-36-6Relevant articles and documents

Probing the catalytic mechanism of s-ribosylhomocysteinase (LuxS) with catalytic intermediates and substrate analogues

Gopishetty, Bhaskar,Zhu, Jinge,Rajan, Rakhi,Sobczak, Adam J.,Wnuk, Stanislaw F.,et al.

body text, p. 1243 - 1250 (2009/06/28)

S-Ribosylhomocysteinase (LuxS) cleaves the thioether bond in S-ribosylhomocysteine (SRH) to produce homocysteine (Hcys) and 4,5-dihydroxy-2,3-pentanedione (DPD), the precursor of the type II bacterial quorum sensing molecule (AI-2). The catalytic mechanis

The Use of Grignard Reagents in the Synthesis of Carbohydrates. III. The One-way Anomerization of Methyl Glycofuranosides and the Opening of Their Furanose Rings

Kawana, Masajiro,Kuzuhara, Hiroyoshi,Emoto, Sakae

, p. 1492 - 1504 (2007/10/02)

The anomerization of methyl glycofuranoside derivatives with methylmagnesium iodide or t-butylmagnesium bromide occurred in a one-way manner.For example, methyl 5-O-benzyl-β-D-ribofuranoside (3β) was converted into the corresponding α-anomer (3α) in a 95p

HYDROGENOLYSIS OF 3,5-O-BENZYLIDENE ACETALS WITH THE LiAlH4-AlCl3 REAGENT IN METHYL D-XYLOFURANOSIDES

Liptak, Andras,Neszmelyi, Andras,Kovac, Pavol,Hirsch, Jan

, p. 2379 - 2382 (2007/10/02)

The hydrogenolysis of methyl 3,5-O-benzylidene-α- and -β-D-xylofuranoside derivatives with the LiAlH4-AlCl3 reagent gave 5-benzyl ethers as main products.In some cases the attack of the reagent occured at the ring oxygen of the furanoside skeleton to yiel

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