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CAS

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128596-96-3

benzyl O--(2->3)-2,4,6-tri-O-benzyl-β-D-galactopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 128596-96-3 Structure

  • Basic information

    1. Product Name: benzyl O--(2->3)-2,4,6-tri-O-benzyl-β-D-galactopyranoside
    2. Synonyms: benzyl O--(2->3)-2,4,6-tri-O-benzyl-β-D-galactopyranoside
    3. CAS NO:128596-96-3
    4. Molecular Formula:
    5. Molecular Weight: 1206.44
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 128596-96-3.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: benzyl O--(2->3)-2,4,6-tri-O-benzyl-β-D-galactopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: benzyl O--(2->3)-2,4,6-tri-O-benzyl-β-D-galactopyranoside(128596-96-3)
    11. EPA Substance Registry System: benzyl O--(2->3)-2,4,6-tri-O-benzyl-β-D-galactopyranoside(128596-96-3)

  • 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: 128596-96-3(Hazardous Substances Data)

128596-96-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 128596-96-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,5,9 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 128596-96:
(8*1)+(7*2)+(6*8)+(5*5)+(4*9)+(3*6)+(2*9)+(1*6)=173
173 % 10 = 3
So 128596-96-3 is a valid CAS Registry Number.

128596-96-3Downstream Products

128596-96-3Relevant articles and documents

HIGHLY STEREOSELECTIVE GLYCOSYLATION OF SIALIC ACID AIDED BY STEREOCONTROLLING AUXILIARIES

Ito, Yukishige,Ogawa, Tomoya

, p. 89 - 102 (1990)

α-Selective glycosylation of sialic acid was achieved by using a sialic acid donor which carries a stereocontrolling auxiliary such as selenide or sulfide group at C-3 position.

HIGHLY STEREOSELECTIVE GLYCOSYLATION OF N-ACETYLNEURAMINIC ACID AIDED BY A PHENYLTHIO SUBSTITUENT AS A STEREOCONTROLLING AUXILIARY

Ito, Yukishige,Ogawa, Tomoya

, p. 3987 - 3990 (2007/10/02)

The 2-halo-3β-phenylthio derivatives of N-acetylneuraminic acid afforded 2α-glycosides in a high stereoselectivity.

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